Bicycloheteroaryl compounds as P2X7 modulators and uses thereof

ABSTRACT

Bicycloheteroaryl compounds are disclosed that have a formula represented by the following: 
                         
The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a National Stage Application claiming the priority of co-pending PCT Application No. PCT/US2007/006700 filed Mar. 16, 2007, which in turn, claims priority from U.S. Provisional application Ser. Nos.: 60/783,590; 60/783,748; 60/783,121; and 60/782,923, all filed Mar. 16, 2006; Ser. No. 60/831,416, filed Jul. 17, 2006; Ser. No. 60/846,993, filed Sep. 25, 2006; and Ser. No. 60/918,261, filed Mar. 15, 2007. Applicants claim the benefits of 35 U.S.C. §120 as to the PCT application and priority under 35 U.S.C. §119 as to the said U.S. Provisional applications, and the entire disclosures of all applications are incorporated herein by reference in their entireties.

FIELD OF THE INVENTION

This invention relates to novel compounds of the class bicycloheteroaryls that are capable of modulating P2X₇ receptor activity, and to pharmaceutical compositions containing such compounds. This invention also relates to methods for preventing and/or treating conditions that are causally related to aberrant P2X₇ activity, such as inflammation-related conditions in mammals, comprising (but not limited to) rheumatoid arthritis, osteoarthritis, Parkinson's disease, uveitis, asthma, cardiovascular conditions including myocardial infarction, the treatment and prophylaxis of pain syndromes (acute and chronic or neuropathic), traumatic brain injury, acute spinal cord injury, neurodegenerative disorders, inflammatory bowel disease and autoimmune disorders, using the compounds and pharmaceutical compositions of the invention.

BACKGROUND OF THE INVENTION

Cell surface receptors for ATP can be divided into metabotropic (P2Y/P2U) and ionotropic (P2X) classes. The metabotropic class belongs to the superfamily of G protein-coupled receptors, with seven transmembrane segments. The ionotropic class members (P2-X₁-P2X₆) are ligand-gated ion channels, currently thought to be multisubunit proteins with two transmembrane domains per subunit (Buell et al, Europ. J. Neurosci. 8:2221 (1996)). P2Z receptors have been distinguished from other P2 receptors in three primary ways (Buisman et al, Proc. Natl. Acad. Sci. USA 85:7988 (1988); Cockcroft et al, Nature 279:541 (1979); Steinberg et al, J. Biol. Chem. 262:3118 (1987)). First, activation of P2Z receptors leads not only to an inward ionic current, but also to cell permeabilization. Second, 3′-O-(4-benzoyl)benzoyl ATP (BZATP) is the most effective agonist, and ATP itself is of rather low potency. Third, responses are strongly inhibited by extracellular magnesium ions, that has been interpreted to indicate that ATP⁴—is the active agonist (DiVirgilio, Immunol. Today 16:524 (1995)).

A seventh member of the P2X receptor family has been isolated from a rat cDNA library and, when expressed in human embryonic kidney (HEK293) cells, exhibits the above three properties (Surprenant et al, Science 272:735 (1996)). This receptor (rP2X₇) thus corresponds to the P2Z receptor. rP2X₇ is structurally related to other members of the P2X family but it has a longer cytoplasmic C-terminus domain (there is 35-40% amino acid identity in the corresponding region of homology, but the C-terminus is 239 amino acids long in the rP2X₇ receptor compared with 27-20 amino acids in the others). The rP2X₇ receptor functions both as a channel permeable to small cations and as a cytolytic pore. Brief applications of ATP (1-2s) transiently open the channel, as is the case of other P2X receptors. Repeated or prolonged applications of agonist cause cell permeabilization reducing the extracellular magnesium concentration potentiates this effect. The unique C-terminal domain of rP2X₇ is required for cell permeabilization and the lytic actions of ATP (Suprenant et al, Science 272:735 (1996)).

The P2Z/rP2X₇ receptor has been implicated in lysis of antigen-presenting cells by cytotoxic T lymphocytes, in the mitogenic stimulation of human T lymphocytes, as well as in the formation of multinucleated giant cells (Blanchard et al, Blood 85:3173 (1995); Falzoni et al, J. Clin. Invest. 95:1207 (1995); Baricolrdi et al, Blood 87:682 (1996)). Certain functional differences exist between rodent and man (Hickman et al, Blood 84:2452 (1994)). The human macrophage P2X₇ receptor (P2X₇) has now been cloned and its functional properties determined (Rassendren et al, J. Biol. Chem. 272:5482 (1997). When compared with the rat P2X₇ receptor, elicited cation-selective currents in the human P2X₇ receptor required higher concentrations of agonists, were more potentiated by removal of extracellular magnesium ions, and revised more rapidly on agonist removal. Expression of chimeric molecules indicated that some of the differences between rat and human P2X₇ receptors could be revised by exchanging the respective C-terminal domains of the receptor proteins.

It has been reported that certain compounds act as P2X₇ antagonists. For example, WO99/29660 and WO99/29661 disclose that certain adamantane derivatives exhibit P2X₇ antagonistic activity having therapeutic efficacy in the treatment of rheumatoid arthritis and psoriasis. Similarly, WO99/29686 discloses that certain heterocyclic derivatives are P2X₇ receptor antagonists and are useful as immunosuppressive agents and treating rheumatoid arthritis, asthma, septic shock and atherosclerosis. Finally, WO00/71529 discloses certain substituted phenyl compounds exhibiting immunosuppressing activity. All of the references described herein are incorporated herein by reference in their entirety.

A need therefore exists for therapeutic agents, and corresponding pharmaceutical compositions and related methods of treatment, that address the conditions causally related to aberrant P2X₇ activity, and it is toward the fulfillment and satisfaction of that need, that the present invention is directed.

SUMMARY OF THE INVENTION

Bicycloaryl derivatives of formulae I-XIIj, and their pharmaceutical compositions are disclosed as therapeutic agents useful for the treatment of conditions in mammals associated with abnormal or aberrant activity of the P2X₇ receptor, including inflammatory-mediated conditions such as (but not limited to) arthritis, myocardial infarction, the treatment and prophylaxis of pain syndromes (acute and chronic [neuropathic]), traumatic brain injury, acute spinal cord injury, neurodegenerative disorders, inflammatory bowel disease and immune dysfunctions such as autoimmune disorders.

It has now been found that the present bicycloheteroaryl compounds are capable of mediating the activity of the P2X₇ receptor. This finding leads to novel compounds having therapeutic value. It also leads to pharmaceutical compositions having the compounds of the present invention as active ingredients and to their use to treat, prevent or ameliorate a range of conditions in mammals such as but not limited to inflammation of various genesis or etiology, for example rheumatoid arthritis, cardiovascular disease, inflammatory bowel disease, acute, chronic, inflammatory and neuropathic pain, dental pain and headache (such as migraine, cluster headache and tension headache) and other conditions causally related to inflammation or immune dysfunction.

The compounds of the present invention are also useful for the treatment of inflammatory pain and associated hyperalgesia and allodynia. They are also useful for the treatment of neuropathic pain and associated hyperalgesis and allodynia (e.g. trigeminal or herpetic neuralgia, diabetic neuropathy, causalgia, sympathetically maintained pain and deafferentation syndromes such as brachial plexus avulsion). The compounds of the present invention are also useful as anti-inflammatory agents for the treatment of arthritis, and as agents to treat Parkinson's Disease, uveitis, asthma, myocardial infarction, traumatic brain injury, spinal cord injury, neurodegenerative disorders, inflammatory bowel disease and autoimmune disorders, renal disorders, obesity, eating disorders, cancer, schizophrenia, epilepsy, sleeping disorders, cognition, depression, anxiety, blood pressure, lipid disorders, and atherosclerosis.

In one aspect, this invention provides bicycloheteroaryl compounds which are capable of modulating the activity of the P2X₇ receptor, in vivo. In a further aspect, the compounds of the invention are capable of antagonizing (suppressing or inhibiting) the activity of the P2X₇ receptor, and thereby treating those conditions, representative ones of which are causally related to aberrant P2X₇ activity.

The compounds of the present invention may show low toxicity, good absorption, good half-life, good solubility, low protein binding affinity, low drug-drug interaction, low inhibitory activity at the HERG channel, low QT prolongation and good metabolic stability.

Accordingly, in a first aspect of the invention, bicycloheteroaryl compounds are disclosed that are capable of capable of modulating the activity of the P2X₇ receptor in vivo, having a formula (I):

-   -   wherein     -   B and Y are independently selected from CR^(2a) and         CR^(2a)R^(2b);     -   W, W′ and Z are independently selected from CR⁴ and N, provided         that all three of W, W′ and Z are not N at the same time;     -   L¹ is substituted or unsubstituted C₁-C₅ alkylene;     -   n is 0, 1, 2, 3 or 4;     -   R¹ is selected from a substituted or unsubstituted 3-13 membered         cycloalkyl, heterocycloalkyl, aryl and heteroaryl ring;     -   each of R^(2a), R^(2b), R^(2′) and R^(2″) is independently         selected from hydrogen, halo, and substituted or unsubstituted         C₁-C₆ alkyl; or any of R^(2′) and R^(2″) join together to form a         cycloalkyl or cycloheteroalkyl ring of 3-7 atoms;     -   R³ is hydrogen or a functional group selected from acyl,         substituted acyl, substituted or unsubstituted acylamino,         substituted or unsubstituted alkylamino, substituted or         unsubstituted dialkylamino, substituted or unsubstituted         alkylthio, substituted or unsubstituted alkoxy, alkoxycarbonyl,         substituted alkoxycarbonyl, substituted or unsubstituted         alkylarylamino, arylalkyloxy, substituted arylalkyloxy, aryl,         substituted aryl, arylalkyl, substituted or unsubstituted         sulfoxide, substituted or unsubstituted sulfone, substituted or         unsubstituted sulfanyl, substituted or unsubstituted         aminosulfonyl, substituted or unsubstituted arylsulfonyl,         sulfuric acid, sulfuric acid ester, substituted or unsubstituted         carbamoyl, cyano, substituted or unsubstituted cycloalkyl,         substituted or unsubstituted cycloheteroalkyl, halo,         heteroaryloxy, substituted or unsubstituted heteroaryl,         substituted or unsubstituted heteroalkyl, nitro, and thio;         provided that R³ is other than hydrogen bond donor group;     -   R⁴ is independently selected from H, alkyl, substituted alkyl,         acyl, substituted acyl, substituted or unsubstituted acylamino,         substituted or unsubstituted alkylamino, substituted or         unsubstituted alkylthio, substituted or unsubstituted alkoxy,         alkoxycarbonyl, substituted alkoxycarbonyl, substituted or         unsubstituted alkylarylamino, arylalkyloxy, substituted         arylalkyloxy, amino, aryl, substituted aryl, arylalkyl,         substituted or unsubstituted sulfoxide, substituted or         unsubstituted sulfone, substituted or unsubstituted sulfanyl,         substituted or unsubstituted aminosulfonyl, substituted or         unsubstituted arylsulfonyl, sulfuric acid, sulfuric acid ester,         substituted or unsubstituted dihydroxyphosphoryl, substituted or         unsubstituted aminodihydroxyphosphoryl, azido, carboxy,         substituted or unsubstituted carbamoyl, cyano, substituted or         unsubstituted cycloalkyl, substituted or unsubstituted         cycloheteroalkyl, substituted or unsubstituted dialkylamino,         halo, heteroaryloxy, substituted or unsubstituted heteroaryl,         substituted or unsubstituted heteroalkyl, hydroxy, nitro, and         thio;     -   and the dotted bond is a single or a double bond;     -   or a pharmaceutically acceptable salt, solvate or prodrug         thereof;     -   and stereoisomers, isotopic variants and tautomers thereof.

In a further embodiment, with respect to compounds of formulae I, n is 0-4. In another embodiment, n is 0-2. In a particular embodiment, n is 1.

In a further embodiment, with respect to compounds of formula I, L¹ is a C₁-C₅ alkylene group unsubstituted or substituted by one or more substituents selected from alkyl, oxo, aryl, hydroxyl, or hydroxyalkyl.

In a further embodiment, with respect to compounds of formula I, B and Y are independently selected from CR^(2a) and CR^(2a)R^(2b).

In a further embodiment, with respect to compounds of formula I B and Y are independently selected from CR^(2a)R^(2b) and the dotted bond is a single bond.

In a further embodiment, with respect to compounds of formula I, B and Y may all represent CH₂ and the dotted bond is a single bond.

In a further embodiment, with respect to compounds of formula I, B and Y are independently selected from CR^(2a) and the dotted bond is a double bond.

In a further embodiment, with respect to compounds of formula I, B and Y may all represent CH and the dotted bond is a double bond.

In a further embodiment, with respect to compounds of formula I, n is 0, 1 or 2. In one particular embodiment, n is 1.

In another embodiment, with respect to compounds of formula I, each of R^(2′) and R^(2″) of the

group is H or Me. In one particular embodiment, each of R^(2′) and R^(2″) is H.

In a further embodiment, with respect to compounds of formula I, one of R^(2′) and R^(2″) of the

group may be selected from Me, Et, halo and Cl, and the other is H.

In a further embodiment, with respect to compounds of formula I, R¹ is substituted or unsubstituted aryl. In one particular embodiment, R¹ is substituted or unsubstituted phenyl.

In a further embodiment, with respect to compounds of formula I, R¹ is substituted or unsubstituted cycloalkyl. In another embodiment, R¹ is substituted or unsubstituted adamantyl. In yet another embodiment, R¹ is substituted or unsubstituted cyclohexyl or cycloheptyl.

In a further embodiment, with respect to compounds of formula I, each of W and W′ is N.

In a further embodiment, with respect to compounds of formula I, each of W, Z and W′ is CR⁴. In one particular embodiment, each of W, Z and W′ is CH.

In a further embodiment, with respect to compounds of formula I, each of W and Z is CR⁴, W′ is CR⁵ and R⁵ is H, alkyl, cycloalkyl or halo. In one embodiment. R⁵ is halo or alkyl. In a particular embodiment, R⁵ is H or halo. In a yet further particular embodiment, R⁵ is H, Cl, F, Me or cyclopropyl.

In a further aspect, the present invention provides pharmaceutical compositions comprising a bicycloheteroaryl compound of the invention, and a pharmaceutical carrier, excipient or diluent. In this aspect of the invention, the pharmaceutical composition can comprise one or more of the compounds described herein. Moreover, the compounds of the present invention useful in the pharmaceutical compositions and treatment methods disclosed herein, are all pharmaceutically acceptable as prepared and used.

In a further aspect of the invention, this invention provides a method of treating a mammal susceptible to or afflicted with a condition from among those listed herein, and particularly, such condition as may be associated with e.g. inflammation, such as rheumatoid arthritis, osteoarthritis, uveitis, asthma, myocardial infarction, traumatic brain injury; septic shock, atherosclerosis, chronic pulmonary obstructive disease (COPD), acute spinal cord injury; inflammatory bowel disease and immune dysfunction, including autoimmune disorders, which method comprises administering an effective amount of one or more of the pharmaceutical compositions just described.

In yet another method of treatment aspect, this invention provides a method of treating a mammal susceptible to or afflicted with a condition that is causally related to aberrant P2X₇ receptor activity, and that for example, gives rise to pain responses or that relates to imbalances in the maintenance of basal activity of sensory nerves. The amine compounds of the invention have use as analgesics for the treatment of pain of various geneses or etiology, for example acute, inflammatory pain (such as pain associated with osteoarthritis and rheumatoid arthritis); various neuropathic pain syndromes (such as post-herpetic neuralgia, trigeminal neuralgia, reflex sympathetic dystrophy, diabetic neuropathy, Guillian Barre syndrome, fibromyalgia, phantom limb pain, post-masectomy pain, peripheral neuropathy, HIV neuropathy, and chemotherapy-induced and other iatrogenic neuropathies); visceral pain, (such as that associated with gastroesophageal reflex disease, irritable bowel syndrome, inflammatory bowel disease, pancreatitis, and various gynecological and urological disorders), dental pain and headache (such as migraine, cluster headache and tension headache).

In additional method of treatment aspects, this invention provides methods of treating a mammal susceptible to or afflicted with conditions that are causally related to abnormal activity of the P2X₇ receptor, such as neurodegenerative diseases and disorders including, for example, Parkinson's disease, multiple sclerosis; diseases and disorders which are mediated by or result in neuroinflammation such as, for example traumatic brain injury and encephalitis; centrally-mediated neuropsychiatric diseases and disorders such as, for example depression mania, bipolar disease, anxiety, schizophrenia, eating disorders, sleep disorders and cognition disorders; epilepsy and seizure disorders; prostate, bladder and bowel dysfunction such as, for example urinary incontinence, urinary hesitancy, rectal hypersensitivity, fecal incontinence, benign prostatic hypertrophy and inflammatory bowel disease; respiratory and airway disease and disorders such as, for example, allergic rhinitis, asthma and reactive airway disease and chronic obstructive pulmonary disease; diseases and disorders which are mediated by or result in inflammation such as, for example rheumatoid arthritis and osteoarthritis, myocardial infarction, various autoimmune diseases and disorders, uveitis and atherosclerosis; itch/pruritus such as, for example psoriasis; obesity; lipid disorders; cancer; blood pressure; spinal cord injury; and cardiovascular and renal disorders method comprises administering an effective condition-treating or condition-preventing amount of one or more of the pharmaceutical compositions just described.

In additional aspects, this invention provides methods for synthesizing the compounds of the invention, with representative synthetic protocols and pathways disclosed later on herein.

Accordingly, it is a principal object of this invention to provide a novel series of compounds, which can modify the activity of the P2X₇ receptor and thus avert or treat any maladies that may be causally related thereto.

It is further an object of this invention to provide a series of compounds that can treat or alleviate maladies or symptoms of same, such as pain and inflammation, that may be causally related to the activation of the P2X₇ receptor.

A still further object of this invention is to provide pharmaceutical compositions that are effective in the treatment or prevention of a variety of disease states, including the diseases associated with the central nervous system, cardiovascular conditions, chronic pulmonary obstructive disease COPD), inflammatory bowel disease, rheumatoid arthritis, osteoarthritis, and other diseases where an inflammatory component is present.

Other objects and advantages will become apparent to those skilled in the art from a consideration of the ensuing detailed description.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

When describing the compounds, pharmaceutical compositions containing such compounds and methods of using such compounds and compositions, the following terms have the following meanings unless otherwise indicated. It should also be understood that any of the moieties defined forth below may be substituted with a variety of substituents, and that the respective definitions are intended to include such substituted moieties within their scope. By way of non-limiting example, such substituents may include e.g. halo (such as fluoro, chloro, bromo), —CN, —CF₃, —OH, —OCF₃, C₂-C₆ alkenyl, C₃-C₆ alkenyl, C₁-C₆ alkoxy, aryl and di-C₁-C₆ alkylamino. It should be further understood that the terms “groups” and “radicals” can be considered interchangeable when used herein.

“Acyl” refers to a radical —C(O)R²⁰, where R²⁰ is hydrogen, alkyl, cycloalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroalkyl, heteroaryl, heteroarylalkyl as defined herein. Representative examples include, but are not limited to, formyl, acetyl, cylcohexylcarbonyl, cyclohexylmethylcarbonyl, benzoyl, benzylcarbonyl and the like.

“Acylamino” refers to a radical —NR²¹C(O)R²², where R²¹ is hydrogen, alkyl, cycloalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroalkyl, heteroaryl, heteroarylalkyl and R²² is hydrogen, alkyl, alkoxy, cycloalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroalkyl, heteroaryl or heteroarylalkyl, as defined herein. Representative examples include, but are not limited to, formylamino, acetylamino, cyclohexylcarbonylamino, cyclohexylmethyl-carbonylamino, benzoylamino, benzylcarbonylamino and the like.

“Acyloxy” refers to the group —OC(O)R²³ where R²³ is hydrogen, alkyl, aryl or cycloalkyl.

“Substituted alkenyl” includes those groups recited in the definition of “substituted” herein, and particularly refers to an alkenyl group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Alkoxy” refers to the group —OR²⁴ where R²⁴ is alkyl. Particular alkoxy groups include, by way of example, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentoxy, n-hexoxy, 1,2-dimethylbutoxy, and the like.

“Substituted alkoxy” includes those groups recited in the definition of “substituted” herein, and particularly refers to an alkoxy group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, heteroaryl, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Alkoxycarbonylamino” refers to the group —NR²⁵C(O)OR²⁶, where R²⁵ is hydrogen, alkyl, aryl or cycloalkyl, and R²⁶ is alkyl or cycloalkyl.

“Alkyl” refers to monovalent saturated alkane radical groups particularly having up to about 11 carbon atoms, more particularly as a lower alkyl, from 1 to 8 carbon atoms and still more particularly, from 1 to 6 carbon atoms. The hydrocarbon chain may be either straight-chained or branched. This term is exemplified by groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, tert-butyl, n-octyl, tert-octyl and the like. The term “lower alkyl” refers to alkyl groups having 1 to 6 carbon atoms. The term “alkyl” also includes “cycloalkyls” as defined below.

“Substituted alkyl” includes those groups recited in the definition of “substituted” herein, and particularly refers to an alkyl group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, heteroaryl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂—, and aryl-S(O)₂—.

“Alkylene” refers to divalent saturated alkene radical groups having 1 to 11 carbon atoms and more particularly 1 to 6 carbon atoms which can be straight-chained or branched. This term is exemplified by groups such as methylene (—CH₂—), ethylene (—CH₂CH₂—), the propylene isomers (e.g., —CH₂CH₂CH₂— and —CH(CH₃)CH₂—) and the like.

“Substituted alkylene” includes those groups recited in the definition of “substituted” herein, and particularly refers to an alkylene group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, amino-carbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Alkenyl” refers to monovalent olefinically unsaturated hydrocarbyl groups preferably having 2 to 11 carbon atoms, particularly, from 2 to 8 carbon atoms, and more particularly, from 2 to 6 carbon atoms, which can be straight-chained or branched and having at least 1 and particularly from 1 to 2 sites of olefinic unsaturation. Particular alkenyl groups include ethenyl (—CH═CH₂), n-propenyl (—CH₂CH═CH₂), isopropenyl (—C(CH₃)═CH₂), vinyl and substituted vinyl, and the like.

“Alkenylene” refers to divalent olefinically unsaturated hydrocarbyl groups particularly having up to about 11 carbon atoms and more particularly 2 to 6 carbon atoms which can be straight-chained or branched and having at least 1 and particularly from 1 to 2 sites of olefinic unsaturation. This term is exemplified by groups such as ethenylene (—CH═CH—), the propenylene isomers (e.g., —CH═CHCH₂— and —C(CH₃)═CH— and —CH═C(CH₃)—) and the like.

“Alkynyl” refers to acetylenically or alkynically unsaturated hydrocarbyl groups particularly having 2 to 11 carbon atoms and more particularly 2 to 6 carbon atoms which can be straight-chained or branched and having at least 1 and particularly from 1 to 2 sites of alkynyl unsaturation. Particular non-limiting examples of alkynyl groups include acetylenic, ethynyl (—C≡CH), propargyl (—CH₂C≡CH), and the like.

“Substituted alkynyl” includes those groups recited in the definition of “substituted” herein, and particularly refers to an alkynyl group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Alkanoyl” or “acyl” as used herein refers to the group R²⁷—C(O)—, where R²⁷ is hydrogen or alkyl as defined above.

“Aryl” refers to a monovalent aromatic hydrocarbon group derived by the removal of one hydrogen atom from a single carbon atom of a parent aromatic ring system. Typical aryl groups include, but are not limited to, groups derived from aceanthrylene, acenaphthylene, acephenanthrylene, anthracene, azulene, benzene, chrysene, coronene, fluoranthene, fluorene, hexacene, hexaphene, hexylene, as-indacene, s-indacene; indane, indene, naphthalene, octacene, octaphene, octalene, ovalene, penta-2,4-diene, pentacene, pentalene, pentaphene, perylene, phenalene, phenanthrene, picene, pleiadene, pyrene, pyranthrene, rubicene, triphenylene, trinaphthalene and the like. Particularly, an aryl group comprises from 6 to 14 carbon atoms.

“Substituted Aryl” includes those groups recited in the definition of “substituted” herein, and particularly refers to an aryl group that may optionally be substituted with 1 or more substituents, for instance from 1 to 5 substituents, particularly 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkenyl, substituted alkenyl, alkoxy, substituted alkoxy, alkoxycarbonyl, alkyl, substituted alkyl, alkynyl, substituted alkynyl, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Fused Aryl” refers to an aryl having two of its ring carbon in common with a second aryl ring or with an aliphatic ring.

“Alkaryl” refers to an aryl group, as defined above, substituted with one or more alkyl groups, as defined above.

“Aralkyl” or “arylalkyl” refers to an alkyl group, as defined above, substituted with one or more aryl groups, as defined above.

“Aryloxy” refers to —O-aryl groups wherein “aryl” is as defined above.

“Alkylamino” refers to the group alkyl-NR²⁸R²⁹, wherein each of R²⁸ and R²⁹ are independently selected from hydrogen and alkyl.

“Arylamino” refers to the group aryl-NR³⁰R³¹, wherein each of R³⁰ and R³¹ are independently selected from hydrogen, aryl and heteroaryl.

“Alkoxyamino” refers to a radical —N(H)OR³² where R³² represents an alkyl or cycloalkyl group as defined herein.

“Alkoxycarbonyl” refers to a radical —C(O)-alkoxy where alkoxy is as defined herein.

“Alkylarylamino” refers to a radical —NR³³R³⁴ where R³³ represents an alkyl or cycloalkyl group and R³⁴ is an aryl as defined herein.

“Alkylsulfonyl” refers to a radical —S(O)₂R³⁵ where R³⁵ is an alkyl or cycloalkyl group as defined herein. Representative examples include, but are not limited to, methylsulfonyl, ethylsulfonyl, propylsulfonyl, butylsulfonyl and the like.

“Alkylsulfinyl” refers to a radical —S(O)R³⁵ where R³⁵ is an alkyl or cycloalkyl group as defined herein. Representative examples include, but are not limited to, methylsulfinyl, ethylsulfinyl, propylsulfinyl, butylsulfinyl and the like.

“Alkylthio” refers to a radical —SR³⁵ where R³⁵ is an alkyl or cycloalkyl group as defined herein that may be optionally substituted as defined herein. Representative examples include, but are not limited to, methylthio, ethylthio, propylthio, butylthio, and the like.

“Amino” refers to the radical —NH₂.

“Substituted amino” includes those groups recited in the definition of “substituted” herein, and particularly refers to the group —N(R³⁶)₂ where each R³⁶ is independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, cycloalkyl, substituted cycloalkyl, and where both R groups are joined to form an alkylene group. When both R groups are hydrogen, —N(R³⁶)₂ is an amino group.

“Aminocarbonyl” refers to the group —C(O)NR³⁷R³⁷ where each R³⁷ is independently hydrogen, alkyl, aryl and cycloalkyl, or where the R³⁷ groups are joined to form an alkylene group.

“Aminocarbonylamino” refers to the group —NR³⁸C(O)NR³⁸R³⁸ where each R³⁸ is independently hydrogen, alkyl, aryl or cycloalkyl, or where two R groups are joined to form an alkylene group.

“Aminocarbonyloxy” refers to the group —OC(O)NR³⁹R³⁹ where each R³⁹ is independently hydrogen, alkyl, aryl or cycloalkyl, or where the R groups are joined to form an alkylene group.

“Arylalkyloxy” refers to an —O-arylalkyl radical where arylalkyl is as defined herein.

“Arylamino” means a radical —NHR⁴⁰ where R⁴⁰ represents an aryl group as defined herein.

“Aryloxycarbonyl” refers to a radical —C(O)—O-aryl where aryl is as defined herein.

“Arylsulfonyl” refers to a radical —S(O)₂R⁴¹ where R⁴¹ is an aryl or heteroaryl group as defined herein.

“Azido” refers to the radical —N₃.

“Bicycloaryl” refers to a monovalent aromatic hydrocarbon group derived by the removal of one hydrogen atom from a single carbon atom of a parent bicycloaromatic ring system. Typical bicycloaryl groups include, but are not limited to, groups derived from indane, indene, naphthalene, tetrahydronaphthalene, and the like. Particularly, an aryl group comprises from 8 to 11 carbon atoms.

“Bicycloheteroaryl” refers to a monovalent bicycloheteroaromatic group derived by the removal of one hydrogen atom from a single atom of a parent bicycloheteroaromatic ring system. Typical bicycloheteroaryl groups include, but are not limited to, groups derived from benzofuran, benzimidazole, benzindazole, benzdioxane, chromene, chromane, cinnoline, phthalazine, indole, indoline, indolizine, isobenzofuran, isochromene, isoindole, isoindoline, isoquinoline, benzothiazole, benzoxazole, naphthyridine, benzoxadiazole, pteridine, purine, benzopyran, benzpyrazine, pyridopyrimidine, quinazoline, quinoline, quinolizine, quinoxaline, benzomorphan, tetrahydroisoquinoline, tetrahydroquinoline, and the like. Preferably, the bicycloheteroaryl group is between 9-11 membered bicycloheteroaryl, with 5-10 membered heteroaryl being particularly preferred. Particular bicycloheteroaryl groups are those derived from benzothiophene, benzofuran, benzothiazole, indole, quinoline, isoquinoline, benzimidazole, benzoxazole and benzdioxane.

“Carbamoyl” refers to the radical —C(O)N(R⁴²)₂ where each R⁴² group is independently hydrogen, alkyl, cycloalkyl or aryl, as defined herein, which may be optionally substituted as defined herein.

“Carboxy” refers to the radical —C(O)OH.

“Carboxyamino” refers to the radical —N(H)C(O)OH.

“Cycloalkyl” refers to cyclic hydrocarbyl groups having from 3 to about 10 carbon atoms and having a single cyclic ring or multiple condensed rings, including fused and bridged ring systems, which optionally can be substituted with from 1 to 3 alkyl groups. Such cycloalkyl groups include, by way of example, single ring structures such as cyclopropyl, cyclobutyl, cyclopentyl, cyclooctyl, 1-methylcyclopropyl, 2-methylcyclopentyl, 2-methylcyclooctyl, and the like, and multiple ring structures such as adamantanyl, and the like.

“Substituted cycloalkyl” includes those groups recited in the definition of “substituted” herein, and particularly refers to a cycloalkyl group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Cycloalkoxy” refers to the group —OR⁴³ where R⁴³ is cycloalkyl. Such cycloalkoxy groups include, by way of example, cyclopentoxy, cyclohexoxy and the like.

“Cycloalkenyl” refers to cyclic hydrocarbyl groups having from 3 to 10 carbon atoms and having a single cyclic ring or multiple condensed rings, including fused and bridged ring systems and having at least one and particularly from 1 to 2 sites of olefinic unsaturation. Such cycloalkenyl groups include, by way of example, single ring structures such as cyclohexenyl, cyclopentenyl, cyclopropenyl, and the like.

“Substituted cycloalkenyl” includes those groups recited in the definition of “substituted” herein, and particularly refers to a cycloalkenyl group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Fused Cycloalkenyl” refers to a cycloalkenyl having two of its ring carbon atoms in common with a second aliphatic or aromatic ring and having its olefinic unsaturation located to impart aromaticity to the cycloalkenyl ring.

“Cyanato” refers to the radical —OCN.

“Cyano” refers to the radical —CN.

“Dialkylamino” means a radical —NR⁴⁴R⁴⁵ where R⁴⁴ and R⁴⁵ independently represent an alkyl, substituted alkyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroaryl, or substituted heteroaryl group as defined herein.

“Ethenyl” refers to substituted or unsubstituted —(C═C)—.

“Ethylene” refers to substituted or unsubstituted —(C—C)—.

“Ethynyl” refers to —(C≡C)—.

“Halo” or “halogen” refers to fluoro, chloro, bromo and iodo. Preferred halo groups are either fluoro or chloro.

“Hydroxy” refers to the radical —OH.

“Nitro” refers to the radical —NO₂.

“Substituted” refers to a group in which one or more hydrogen atoms are each independently replaced with the same or different substituent(s). Typical substituents include, but are not limited to —X, —R⁴⁶, —O⁻, ═O, —OR⁴⁶, —SR⁴⁶, —S⁻, ═S, —NR⁴⁶R⁴⁷, ═NR⁴⁶, —CX₃, —CF₃, —CN, —OCN, —SCN, —NO, —NO₂, ═N₂, —N₃, —S(O)₂O⁻, —S(O)₂OH, —S(O)₂R⁴⁶, —OS(O₂)O⁻, —OS(O)₂R⁴⁶, —P(O)(O⁻)₂, —P(O)(OR⁴⁶)(O⁻), —OP(O)(OR⁴⁶)(OR⁴⁷), —C(O)R⁴⁶, —C(S)R⁴⁶, —C(O)OR⁴⁶, —C(O)NR⁴⁶R⁴⁷, —C(O)O⁻, —C(S)OR⁴⁶, —NR⁴⁸C(O)NR⁴⁶R⁴⁷, —NR⁴⁸C(S)NR⁴⁶R⁴⁷, —NR⁴⁹C(NR⁴⁸)NR⁴⁶R⁴⁷ and —C(NR⁴⁸)NR⁴⁶R⁴⁷, where each X is independently a halogen; each R⁴⁶, R⁴⁷, R⁴⁸ and R⁴⁹ are independently hydrogen, alkyl, substituted alkyl, aryl, substituted alkyl, arylalkyl, substituted alkyl, cycloalkyl, substituted alkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, substituted heteroarylalkyl, —NR⁵⁰R⁵¹, —C(O)R⁵⁰ or —S(O)₂R⁵⁰ or optionally R⁵⁰ and R⁵¹ together with the atom to which they are both attached form a cycloheteroalkyl or substituted cycloheteroalkyl ring; and R⁵⁰ and R⁵¹ are independently hydrogen, alkyl, substituted alkyl, aryl, substituted alkyl, arylalkyl, substituted alkyl, cycloalkyl, substituted alkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl or substituted heteroarylalkyl.

Examples of representative substituted aryls include the following

In these formulae one of R⁵² and R⁵³ may be hydrogen and at least one of R⁵² and R⁵³ is each independently selected from alkyl, alkenyl, alkynyl, cycloheteroalkyl, alkanoyl, alkoxy, aryloxy, heteroaryloxy, alkylamino, arylamino, heteroarylamino, NR⁵⁴COR⁵⁵, NR⁵⁴SOR⁵⁵, NR⁵⁴SO₂R⁵⁷, COOalkyl, COOaryl, CONR⁵⁴R⁵⁵, CONR⁵⁴OR⁵⁵, NR⁵⁴R⁵⁵, SO₂NR⁵⁴R⁵⁵, S-alkyl, S-alkyl, SOalkyl, SO₂alkyl, Saryl, SOaryl, SO₂aryl; or R⁵² and R⁵³ may be joined to form a cyclic ring (saturated or unsaturated) from 5 to 8 atoms, optionally containing one or more heteroatoms selected from the group N, O or S. R⁵⁴, R⁵⁵, and R⁵⁶ are independently hydrogen, alkyl, alkenyl, alkynyl, perfluoroalkyl, cycloalkyl, cycloheteroalkyl, aryl, substituted aryl, heteroaryl, substituted or hetero alkyl or the like.

“Hetero” when used to describe a compound or a group present on a compound means that one or more carbon atoms in the compound or group have been replaced by a nitrogen, oxygen, or sulfur heteroatom. Hetero may be applied to any of the hydrocarbyl groups described above such as alkyl, e.g. heteroalkyl, cycloalkyl, e.g. cycloheteroalkyl, aryl, e.g. heteroaryl, cycloalkenyl, cycloheteroalkenyl, and the like having from 1 to 5, and especially from 1 to 3 heteroatoms.

“Heteroaryl” refers to a monovalent heteroaromatic group derived by the removal of one hydrogen atom from a single atom of a parent heteroaromatic ring system. Typical heteroaryl groups include, but are not limited to, groups derived from acridine, arsindole, carbazole, β-carboline, chromane, chromene, cinnoline, furan, imidazole, indazole, indole, indoline, indolizine, isobenzofuran, isochromene, isoindole, isoindoline, isoquinoline, isothiazole, isoxazole, naphthyridine, oxadiazole, oxazole, perimidine, phenanthridine, phenanthroline, phenazine, phthalazine, pteridine, purine, pyran, pyrazine, pyrazole, pyridazine, pyridine, pyrimidine, pyrrole, pyrrolizine, quinazoline, quinoline, quinolizine, quinoxaline, tetrazole, thiadiazole, thiazole, thiophene, triazole, xanthene, and the like. Preferably, the heteroaryl group is between 5-15 membered heteroaryl, with 5-10 membered heteroaryl being particularly preferred. Particular heteroaryl groups are those derived from thiophene, pyrrole, benzothiophene, benzofuran, indole, pyridine, quinoline, imidazole, oxazole and pyrazine.

Examples of representative heteroaryls include the following:

wherein each Y is selected from carbonyl, N, NR⁵⁸, O, and S; and R⁵⁸ is independently hydrogen, alkyl, cycloalkyl, cycloheteroalkyl, aryl, heteroaryl, heteroalkyl or the like.

As used herein, the term “cycloheteroalkyl” refers to a stable heterocyclic non-aromatic ring and fused rings containing one or more heteroatoms independently selected from N, O and S. A fused heterocyclic ring system may include carbocyclic rings and need only include one heterocyclic ring. Examples of heterocyclic rings include, but are not limited to, piperazinyl, homopiperazinyl, piperidinyl and morpholinyl, and are shown in the following illustrative examples:

wherein each X is selected from CR⁵⁸ ₂, NR⁵⁸, O and S; and each Y is selected from NR⁵⁸, O and S; and R⁵⁸ is independently hydrogen, alkyl, cycloalkyl, cycloheteroalkyl, aryl, heteroaryl, heteroalkyl or the like. These cycloheteroalkyl rings may be optionally substituted with one or more groups selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—. Substituting groups include carbonyl or thiocarbonyl which provide, for example, lactam and urea derivatives.

Examples of representative cycloheteroalkenyls include the following:

wherein each X is selected from CR⁵⁸ ₂, NR⁵⁸, O and S; and each Y is selected from carbonyl, N, NR⁵⁸, O and S; and R⁵⁸ is independently hydrogen, alkyl, cycloalkyl, cycloheteroalkyl, aryl, heteroaryl, heteroalkyl or the like.

Examples of representative aryl having hetero atoms containing substitution include the following:

wherein each X is selected from C—R⁵⁸ ₂, Ne⁵⁸, O and S; and each Y is selected from carbonyl, NR⁵⁸, O and S; and R⁵⁸ is independently hydrogen, alkyl, cycloalkyl, cycloheteroalkyl, aryl, heteroaryl, heteroalkyl or the like.

“Hetero substituent” refers to a halo, O, S or N atom-containing functionality that may be present as an R⁴ in a R⁴C group present as substituents directly on A, B, W, Y or Z of the compounds of this invention' or may be present as a substituent in the “substituted” aryl and aliphatic groups present in the compounds.

Examples of hetero substituents include:

—halo,

—NO₂, —NH₂, —NHR⁵⁹, —N(R⁵⁹)₂,

—NRCOR, —NR⁵⁹SOR⁵⁹, —NR⁵⁹SO₂R⁵⁹, OH, CN,

—CO₂H,

—R⁵⁹—OH, —O—R⁵⁹, —COOR⁵⁹,

—CON(R⁵⁹)₂, —CONROR⁵⁹,

—SO₃H, —R⁵⁹—S, —SO₂N(R⁵⁹)₂,

—S(O)R⁵⁹, —S(O)₂R⁵⁹

wherein each R⁵⁹ is independently an aryl or aliphatic, optionally with substitution. Among hetero substituents containing R⁵⁹ groups, preference is given to those materials having aryl and alkyl R⁵⁹ groups as defined herein. Preferred hetero substituents are those listed above.

“Hydrogen bond donor” group refers to a group containing O—H, N—H functionality. Examples of “hydrogen bond donor” groups include —OH, —NH₂, and —NH—R^(59a) and wherein R⁵⁹a is alkyl, cycloalkyl, aryl, or heteroaryl.

“Dihydroxyphosphoryl” refers to the radical —PO(OH)₂.

“Substituted dihydroxyphosphoryl” includes those groups recited in the definition of “substituted” herein, and particularly refers to a dihydroxyphosphoryl radical wherein one or both of the hydroxyl groups are substituted. Suitable substituents are described in detail below.

“Aminohydroxyphosphoryl” refers to the radical —PO(OH)NH₂.

“Substituted aminohydroxyphosphoryl” includes those groups recited in the definition of “substituted” herein, and particularly refers to an aminohydroxyphosphoryl wherein the amino group is substituted with one or two substituents. Suitable substituents are described in detail below. In certain embodiments, the hydroxyl group can also be substituted.

“Thioalkoxy” refers to the group —SR⁶⁰ where R⁶⁰ is alkyl.

“Substituted thioalkoxy” includes those groups recited in the definition of “substituted” herein, and particularly refers to a thioalkoxy group having 1 or more substituents, for instance from 1 to 5 substituents, and particularly from 1 to 3 substituents, selected from the group consisting of acyl, acylamino, acyloxy, alkoxy, substituted alkoxy, alkoxycarbonyl, alkoxycarbonylamino, amino, substituted amino, aminocarbonyl, aminocarbonylamino, aminocarbonyloxy, aryl, aryloxy, azido, carboxyl, cyano, cycloalkyl, substituted cycloalkyl, halogen, hydroxyl, keto, nitro, thioalkoxy, substituted thioalkoxy, thioaryloxy, thioketo, thiol, alkyl-S(O)—, aryl-S(O)—, alkyl-S(O)₂— and aryl-S(O)₂—.

“Sulfanyl” refers to the radical HS—. “Substituted sulfanyl” refers to a radical such as RS— wherein R is any substituent described herein.

“Sulfonyl” refers to the divalent radical —S(O₂)—. “Substituted sulfonyl” refers to a radical such as R⁶¹—(O₂)S— wherein R⁶¹ is any substituent described herein. “Aminosulfonyl” or “Sulfonamide” refers to the radical H₂N(O₂)S—, and “substituted aminosulfonyl” or “substituted sulfonamide” refers to a radical such as R⁶² ₂N(O₂)S— wherein each R⁶² is independently any substituent described herein.

“Sulfone” refers to the group —SO₂R⁶³. In particular embodiments, R⁶³ is selected from H, lower alkyl, alkyl, aryl and heteroaryl.

“Thioaryloxy” refers to the group —SR⁶⁴ where R⁶⁴ is aryl.

“Thioketo” refers to the group ═S.

“Thiol” refers to the group —SH.

One having ordinary skill in the art of organic synthesis will recognize that the maximum number of heteroatoms in a stable, chemically feasible heterocyclic ring, whether it is aromatic or non aromatic, is determined by the size of the ring, the degree of unsaturation and the valence of the heteroatoms. In general, a heterocyclic ring may have one to four heteroatoms so long as the heteroaromatic ring is chemically feasible and stable.

“Pharmaceutically acceptable” means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopoeia or other generally recognized pharmacopoeia for use in animals, and more particularly in humans.

“Pharmaceutically acceptable salt” refers to a salt of a compound of the invention that is pharmaceutically acceptable and that possesses the desired pharmacological activity of the parent compound. Such salts include: (1) acid addition salts, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or formed with organic acids such as acetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, 3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethane-disulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo[2.2.2]-oct-2-ene-1-carboxylic acid, glucoheptonic acid, 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, and the like; or (2) salts formed when an acidic proton present in the parent compound either is replaced by a metal ion, e.g., an alkali metal ion, an alkaline earth ion, or an aluminum ion; or coordinates with an organic base such as ethanolamine, diethanolamine, triethanolamine, N-methylglucamine and the like. Salts further include, by way of example only, sodium, potassium, calcium, magnesium, ammonium, tetraalkylammonium, and the like; and when the compound contains a basic functionality, salts of non toxic organic or inorganic acids, such as hydrochloride, hydrobromide, tartrate, mesylate, acetate, maleate, oxalate and the like. The term “pharmaceutically acceptable cation” refers to a non toxic, acceptable cationic counter-ion of an acidic functional group. Such cations are exemplified by sodium, potassium, calcium, magnesium, ammonium, tetraalkylammonium cations, and the like.

“Pharmaceutically acceptable vehicle” refers to a diluent, adjuvant, excipient or carrier with which a compound of the invention is administered.

“Preventing” or “prevention” refers to a reduction in risk of acquiring a disease or disorder (i.e., causing at least one of the clinical symptoms of the disease not to develop in a subject that may be exposed to or predisposed to the disease but does not yet experience or display symptoms of the disease).

“Prodrugs” refers to compounds, including derivatives of the compounds of the invention, which have cleavable groups and become by solvolysis or under physiological conditions the compounds of the invention which are pharmaceutically active in vivo. Such examples include, but are not limited to, choline ester derivatives and the like, N-alkylmorpholine esters and the like.

“Solvate” refers to forms of the compound that are associated with a solvent, usually by a solvolysis reaction. Conventional solvents include water, ethanol, acetic acid and the like. The compounds of the invention may be prepared e.g. in crystalline form and may be solvated or hydrated. Suitable solvates include pharmaceutically acceptable solvates, such as hydrates, and further include both stoichiometric solvates and non-stoichiometric solvates.

“Subject” includes humans. The terms “human,” “patient” and “subject” are used interchangeably herein.

“Therapeutically effective amount” means the amount of a compound that, when administered to a subject for treating a disease, is sufficient to effect such treatment for the disease. The “therapeutically effective amount” can vary depending on the compound, the disease and its severity, and the age, weight, etc., of the subject to be treated.

“Treating” or “treatment” of any disease or disorder refers, in one embodiment, to ameliorating the disease or disorder (i.e., arresting or reducing the development of the disease or at least one of the clinical symptoms thereof). In another embodiment “treating” or “treatment” refers to ameliorating at least one physical parameter, which may not be discernible by the subject. In yet another embodiment, “treating” or “treatment” refers to modulating the disease or disorder, either physically, (e.g., stabilization of a discernible symptom), physiologically, (e.g., stabilization of a physical parameter), or both. In yet another embodiment, “treating” or “treatment” refers to delaying the onset of the disease or disorder.

Other derivatives of the compounds of this invention have activity in both their acid and acid derivative forms, but in the acid sensitive form often offers advantages of solubility, tissue compatibility, or delayed release in the mammalian organism (see, Bundgard, H., Design of Prodrugs, pp. 7-9, 21-24, Elsevier, Amsterdam 1985). Prodrugs include acid derivatives well know to practitioners of the art, such as, for example, esters prepared by reaction of the parent acid with a suitable alcohol, or amides prepared by reaction of the parent acid compound with a substituted or unsubstituted amine, or acid anhydrides, or mixed anhydrides. Simple aliphatic or aromatic esters, amides and anhydrides derived from acidic groups pendant on the compounds of this invention are preferred prodrugs. In some cases it is desirable to prepare double ester type prodrugs such as (acyloxy)alkyl esters or ((alkoxycarbonyl)oxy)alkylesters. Preferred are the C₁ to C₈ alkyl, C₂-C₈ alkenyl, aryl, C₇-C₁₂ substituted aryl, and C₇-C₁₂ arylalkyl esters of the compounds of the invention.

As used herein, the term “isotopic variant” refers to a compound that contains unnatural proportions of isotopes at one or more of the atoms that constitute such compound. For example, an “isotopic variant” of a compound can contain one or more non-radioactive isotopes, such as for example, deuterium (²H or D), carbon-13 (¹³C), nitrogen-15 (¹⁵N), or the like. It will be understood that, in a compound where such isotopic substitution is made, the following atoms, where present, may vary, so that for example, any hydrogen may be ²H/D, any carbon may be ¹³C, or any nitrogen may be ¹⁵N, and that the presence and placement of such atoms may be determined within the skill of the art. Likewise, the invention may include the preparation of isotopic variants with radioisotopes, in the instance for example, where the resulting compounds may be used for drug and/or substrate tissue distribution studies. The radioactive isotopes tritium, i.e. ³H, and carbon-14, i.e. ¹⁴C, are particularly useful for this purpose in view of their ease of incorporation and ready means of detection. Further, compounds may be prepared that are substituted with positron emitting isotopes, such as ¹¹C, ¹⁸F, ¹⁵O and ¹³N, and would be useful in Positron Emission Topography (PET) studies for examining substrate receptor occupancy.

All isotopic variants of the compounds provided herein, radioactive or not, are intended to be encompassed within the scope of the invention.

It is also to be understood that compounds that have the same molecular formula but differ in the nature or sequence of bonding of their atoms or the arrangement of their atoms in space are termed “isomers”. Isomers that differ in the arrangement of their atoms in space are termed “stereoisomers”.

Stereoisomers that are not mirror images of one another are termed “diastereomers” and those that are non-superimposable mirror images of each other are termed “enantiomers”. When a compound has an asymmetric center, for example, it is bonded to four different groups, a pair of enantiomers is possible. An enantiomer can be characterized by the absolute configuration of its asymmetric center and is described by the R- and S-sequencing rules of Cahn and Prelog, or by the manner in which the molecule rotates the plane of polarized light and designated as dextrorotatory or levorotatory (i.e., as (+) or (−)-isomers respectively). A chiral compound can exist as either individual enantiomer or as a mixture thereof. A mixture containing equal proportions of the enantiomers is called a “racemic mixture”.

“Tautomers” refer to compounds that are interchangeable forms of a particular compound structure, and that vary in the displacement of hydrogen atoms and electrons. Thus, two structures may be in equilibrium through the movement of π electrons and an atom (usually H). For example, enols and ketones are tautomers because they are rapidly interconverted by treatment with either acid or base. Another example of tautomerism is the aci- and nitro-forms of phenylnitromethane, that are likewise formed by treatment with acid or base.

Tautomeric forms may be relevant to the attainment of the optimal chemical reactivity and biological activity of a compound of interest.

The compounds of this invention may possess one or more asymmetric centers; such compounds can therefore be produced as individual (R)- or (S)-stereoisomers or as mixtures thereof. Unless indicated otherwise, the description or naming of a particular compound in the specification and claims is intended to include both individual enantiomers and mixtures, racemic or otherwise, thereof. The methods for the determination of stereochemistry and the separation of stereoisomers are well-known in the art.

The Compounds

The present invention provides bicycloheteroaryl compounds useful for preventing and/or treating a broad range of conditions, associated with abnormalities in the activity of the P2X₇ receptor, among them, rheumatoid arthritis, Parkinson's disease, uveitis, asthma, cardiovascular conditions such as myocardial infarction, the treatment and prophylaxis of pain syndromes (acute and chronic or neuropathic), traumatic brain injury, acute spinal cord injury, neurodegenerative disorders, inflammatory bowel disease and immune dysfunctions such as autoimmune disorders or conditions, in mammals.

In a first aspect of the invention, bicycloheteroaryl compounds are disclosed that are capable of capable of modulating the activity of the P2X₇ receptor in vivo, having a formula (I):

-   -   wherein     -   B and Y are independently selected from CR^(2a) and CR^(2a)R²b;     -   W, W′ and Z are independently selected from CR⁴ and N, provided         that all three of W, W′ and Z are not N at the same time;     -   L¹ is substituted or unsubstituted C₁-C₅ alkylene;     -   n is 0, 1, 2, 3 or 4;     -   R¹ is selected from a substituted or unsubstituted 3-13 membered         cycloalkyl, heterocycloalkyl, aryl and heteroaryl ring;     -   each of R^(2a), R^(2b), R^(2′) and R^(2″) is independently         selected from hydrogen, halo, and substituted or unsubstituted         C₁-C₆ alkyl; or any of R^(2′) and R^(2″) join together to form a         cycloalkyl or cycloheteroalkyl ring of 3-7 atoms;     -   R³ is hydrogen or a functional group selected from acyl,         substituted acyl, substituted or unsubstituted acylamino,         substituted or unsubstituted alkylamino, substituted or         unsubstituted dialkylamino, substituted or unsubstituted         alkylthio, substituted or unsubstituted alkoxy, alkoxycarbonyl,         substituted alkoxycarbonyl, substituted or unsubstituted         alkylarylamino, arylalkyloxy, substituted arylalkyloxy, aryl,         substituted aryl, arylalkyl, substituted or unsubstituted         sulfoxide, substituted or unsubstituted sulfone, substituted or         unsubstituted sulfanyl, substituted or unsubstituted         aminosulfonyl, substituted or unsubstituted arylsulfonyl,         sulfuric acid, sulfuric acid ester, substituted or unsubstituted         carbamoyl, cyano, substituted or unsubstituted cycloalkyl,         substituted or unsubstituted cycloheteroalkyl, halo,         heteroaryloxy, substituted or unsubstituted heteroaryl,         substituted or unsubstituted heteroalkyl, nitro, and thio;         provided that R³ is other than a hydrogen bond donor group;     -   R⁴ is independently selected from H, alkyl, substituted alkyl,         acyl, substituted acyl, substituted or unsubstituted acylamino,         substituted or unsubstituted alkylamino, substituted or         unsubstituted alkylthio, substituted or unsubstituted alkoxy,         alkoxycarbonyl, substituted alkoxycarbonyl, substituted or         unsubstituted alkylarylamino, arylalkyloxy, substituted         arylalkyloxy, amino, aryl, substituted aryl, arylalkyl,         substituted or unsubstituted sulfoxide, substituted or         unsubstituted sulfone, substituted or unsubstituted sulfanyl,         substituted or unsubstituted aminosulfonyl, substituted or         unsubstituted arylsulfonyl, sulfuric acid, sulfuric acid ester,         substituted or unsubstituted dihydroxyphosphoryl, substituted or         unsubstituted aminodihydroxyphosphoryl, azido, carboxy,         substituted or unsubstituted carbamoyl, cyano, substituted or         unsubstituted cycloalkyl, substituted or unsubstituted         cycloheteroalkyl, substituted or unsubstituted dialkylamino,         halo, heteroaryloxy, substituted or unsubstituted heteroaryl,         substituted or unsubstituted heteroalkyl, hydroxy, nitro, and         thio;     -   and the dotted bond is a single or a double bond;     -   or a pharmaceutically acceptable salt, solvate or prodrug         thereof;     -   and stereoisomers, isotopic variants and tautomers thereof.

In a further embodiment, with respect to compounds of formulae I, n is 0-4. In another embodiment, n is 0-2. In a particular embodiment, n is 1.

In a further embodiment, with respect to compounds of formula I, L¹ is a C₁-C₅ alkylene group unsubstituted or substituted by one or more substituents selected from alkyl, oxo, aryl, hydroxyl, or hydroxyalkyl.

In a further embodiment, with respect to compounds of formula I, B and Y are independently selected from CR^(2a) and CR^(2a)R^(2b).

In a further embodiment, with respect to compounds of formula I, B and Y are independently selected from CR^(2a)R^(2b) and the dotted bond is a single bond.

In a further embodiment, with respect to compounds of formula I, B and Y may all represent CH₂ and the dotted bond is a single bond.

In a further embodiment, with respect to compounds of formula I, B and Y are independently selected from CR^(2a) and the dotted bond is a double bond.

In a further embodiment, with respect to compounds of formula I, B and Y may all represent CH and the dotted bond is a double bond.

In a further embodiment, with respect to compounds of formula I, n is 0, 1 or 2. In one particular embodiment, n is 1.

In another embodiment, with respect to compounds of formula I, each of R^(2′) and R^(2″) of the

group is H or Me. In one particular embodiment, each of R^(2′) and R^(2″) is H.

In a further embodiment, with respect to compounds of formula I, one of R^(2′) and R^(2″) of the

group may be selected from Me, Et, halo and Cl, and the other is H.

In a further embodiment, with respect to compounds of formula I, R¹ is substituted or unsubstituted aryl. In one particular embodiment, R¹ is substituted or unsubstituted phenyl.

In a further embodiment, with respect to compounds of formula I, R¹ is substituted or unsubstituted cycloalkyl. In another embodiment, R¹ is substituted or unsubstituted adamantyl. In yet another embodiment, R¹ is substituted or unsubstituted cyclohexyl or cycloheptyl.

In a further embodiment, with respect to compounds of formula I, each of W and W′ is N.

In a further embodiment, with respect to compounds of formula I, each of W, Z and W′ is CR⁴. In one particular embodiment, each of W, Z and W′ is CH.

In a further embodiment, with respect to compounds of formula I, each of W and Z is CR⁴, W′ is CR⁵ and R⁵ is selected from alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl and halo. In one particular embodiment, R⁵ is selected from Me, cyclopropyl, Cl, F and CF₃.

In another embodiment, with respect to compounds of formula I, the compound is according to formula II, III or IV:

-   -   wherein     -   W is CR⁴; Z is CR⁴;     -   L¹, R¹ R^(2′), R^(2″), R³ and R⁴ are as described for formula I;     -   and R⁵ is selected from H, alkyl, substituted alkyl, acyl,         substituted acyl, substituted or unsubstituted acylamino,         substituted or unsubstituted alkylamino, substituted or         unsubstituted alkylthio, substituted or unsubstituted alkoxy,         alkoxycarbonyl, substituted alkoxycarbonyl, substituted or         unsubstituted alkylarylamino, arylalkyloxy, substituted         arylalkyloxy, amino, aryl, substituted aryl, arylalkyl,         substituted or unsubstituted sulfoxide, substituted or         unsubstituted sulfone, substituted or unsubstituted sulfanyl,         substituted or unsubstituted aminosulfonyl, substituted or         unsubstituted arylsulfonyl, sulfuric acid, sulfuric acid ester,         substituted or unsubstituted dihydroxyphosphoryl, substituted or         unsubstituted aminodihydroxyphosphoryl, azido, carboxy,         substituted or unsubstituted carbamoyl, cyano, substituted or         unsubstituted cycloalkyl, substituted or unsubstituted         cycloheteroalkyl, substituted or unsubstituted dialkylamino,         halo, heteroaryloxy, substituted or unsubstituted heteroaryl,         substituted or unsubstituted heteroalkyl, hydroxy, nitro, and         thio;     -   or a pharmaceutically acceptable salt, solvate or prodrug         thereof;     -   and stereoisomers, isotopic variants and tautomers thereof.

In another embodiment, with respect to compounds of formulae III-IV each of R^(2′) and R^(2″) is H.

In another embodiment, with respect to compounds of formulae III-IV, R^(2′) is halo; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae III-IV, R^(2′) is Cl or F; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae III-IV, R^(2′) is Me or Et; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae III-IV, each of R^(2′) and R^(2″) is Me.

In a more particular embodiment, with respect to compounds of formulae III-IV, R^(2′) is Me; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is substituted or unsubstituted aryl.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is substituted or unsubstituted phenyl or naphthalene.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is substituted or unsubstituted naphthalene.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is unsubstituted naphthalene.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is substituted or unsubstituted phenyl.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is substituted or unsubstituted heteroaryl.

In another embodiment, with respect to compounds of formulae II-IV, each of R¹ is substituted or unsubstituted pyridyl, quinoline, benzodioxole, benzodioxane, benzofuran, benzothiophene, and benzodioxepine.

In another embodiment, with respect to compounds of formula I, the compound is according to formula V, VI or VII:

-   -   wherein     -   W is CR⁴; Z is CR⁴;     -   L¹, R¹ R^(2′), R^(2″), R³ and R⁴ are as described for formula I;         R⁵ is as described for formulae II-IV;     -   R^(4a) is selected from H, alkyl, substituted alkyl, acyl,         substituted acyl, substituted or unsubstituted acylamino,         substituted or unsubstituted alkylamino, substituted or         unsubstituted alkylthio, substituted or unsubstituted alkoxy,         aryloxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted         or unsubstituted alkylarylamino, arylalkyloxy, substituted         arylalkyloxy, amino, aryl, substituted aryl, arylalkyl,         substituted or unsubstituted sulfoxide, substituted or         unsubstituted sulfone, substituted or unsubstituted sulfanyl,         substituted or unsubstituted aminosulfonyl, substituted or         unsubstituted arylsulfonyl, sulfuric acid, sulfuric acid ester,         substituted or unsubstituted dihydroxyphosphoryl, substituted or         unsubstituted aminodihydroxyphosphoryl, azido, carboxy,         substituted or unsubstituted carbamoyl, cyano, substituted or         unsubstituted cycloalkyl, substituted or unsubstituted         cycloheteroalkyl, substituted or unsubstituted dialkylamino,         halo, heteroaryloxy, substituted or unsubstituted heteroaryl,         substituted or unsubstituted heteroalkyl, hydroxy, nitro, and         thio; and m is selected from 0-5;     -   or a pharmaceutically acceptable salt, solvate or prodrug         thereof;     -   and stereoisomers, isotopic variants and tautomers thereof.

With respect to the compounds of the invention wherein m is 0-5 as set forth above, and at any and all locations herein, it is to be understood that when m=0, the ring is unsubstituted.

In one embodiment, with respect to compounds of formulae VI-VII, each of R^(2′) and R^(2″) is H.

In another embodiment, with respect to compounds of formulae VI-VII, R^(2′) is halo; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae VI-VII, R^(2′) is Cl or F; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae VI-VII, R^(2′) is Me or Et; and R^(2″) is H.

In another embodiment, with respect to compounds of formulae VI-VII, each of R^(2′) and R^(2″) is Me.

In a more particular embodiment, with respect to compounds of formulae VI-VII, R^(2′) is Me; and R^(2″) is H.

In another embodiment, with respect to compounds of formula I, the compound is according to formula VIII, IX or X:

wherein

-   W is CR⁴; Z is CR⁴; -   L¹, R³ and R⁴ are as described for formula I; R⁵ is as described for     formulae II-IV; m and R^(4a) are as described for formulae V-VII;     R^(2′) is H or Me; Cy is adamantyl, cyclohexyl or cycloheptyl; and     each R^(4b) is independently selected from C₁-C₄ alkyl and hydroxy;     or a pharmaceutically acceptable salt, solvate or prodrug thereof;     and stereoisomers, isotopic variants and tautomers thereof.

In one embodiment, with respect to compounds of formulae V-X, R is H or

Me. In another embodiment, R^(2′) is Me. In one particular embodiment, R^(2′) is H.

In another embodiment, with respect to compounds of formulae V-X, in is 1, 2 or 3.

In another embodiment, with respect to compounds of formulae V-X, m is 1 or 2. In a particular embodiment m is 1.

In another embodiment, with respect to compounds of formulae V-X, each of R^(4a) is independently selected from Me, Et, Ph, Cl, F, Br, CN, OH, OMe, OEt, OPh, COPh, CF₃, CHF₂, OCF₃, i-Pr, i-Bu, t-Bu, SMe, CH═CH—CO₂H, SOMe, SO₂Me, SO₃H, SO₃Me, and pyridyl.

In another embodiment, with respect to compounds of formulae I-X, L¹ is a C₁-C₅ alkylene group.

In another embodiment, with respect to compounds of formulae I-X, L¹ is a C₁-C₅ alkylene group unsubstituted or substituted by one or more substituents selected from alkyl, hydroxyl, oxo and hydroxyalkyl.

In another embodiment, with respect to compounds of formulae I-X, L¹ is an ethylene group unsubstituted or substituted by one or more substituents selected from Me, Et, i-Pr, hydroxy, and hydroxymethyl.

In another embodiment, with respect to compounds of formulae I-X, L¹ is a methylene group unsubstituted or substituted by one or more substituents selected from Me, Et, i-Pr, and hydroxymethyl.

In another embodiment, with respect to compounds of formulae I-X, R³ is selected from alkyl, dialkylamino, acyloxy, alkoxy, and —SO₂-alkyl.

In another embodiment, with respect to compounds of formulae I-X, R³ is selected from t-Bu, NMe2, SO₂Me, OMe, and OCOMe.

In another embodiment, with respect to compounds of formulae I-X, R³ is substituted or unsubstituted aryl, heteroaryl, cycloalkyl or cycloheteroalkyl.

In another embodiment, with respect to compounds of formulae I-X, R³ is substituted or unsubstituted phenyl, pyridyl, pyran, tetrahydropyran, piperidine, morpholine, pyrrolidine, pyrrolidinone and benzodioxane

In another embodiment, with respect to compounds of formulae I-X, the group -L₁-R³ is selected from

In another embodiment, with respect to compounds of formula I, the compound is according to formula XIa, XIb, XIc, XId, XIe, XIf, XIg, XIh or XIj:

wherein m and R^(4a) are as described for formulae V-VII; and R⁵ is selected from H, alkyl, or halo.

In one embodiment, with respect to compounds of formulae V-XIj, m is 1, 2 or 3.

In another embodiment, with respect to compounds of formulae V-XIj, m is 1 or 2. In a particular embodiment m is 2.

In another embodiment, with respect to compounds of V-XIj, each of R^(4a) is independently selected from Me, Et, Ph, Cl, F, Br, CN, OH, OMe, OEt, OPh, COPh, CF₃, CHF₂, OCF₃, i-Pr, i-Bu, t-Bu, SMe, CH═CH—CO₂H, SOMe, SO₂Me, SO₃H, SO₃Me, and pyridyl.

In another embodiment, with respect to compounds of V-XIj, m is 1 and R^(a) is CF₃.

In another embodiment, with respect to compounds of V-XIj, m is 2 and R^(4a) is F and CF₃.

In another embodiment, with respect to compounds of V-XIj, m is 2 and R^(4a) is F and Cl.

In another embodiment, with respect to compounds of formula I, the compound is according to formula XIIa, XIIb, XIIc, XIId, XIIe, XIIf, XIIg, XIIh or XIIj:

wherein Cy is cyclohexyl or cycloheptyl; R^(4a) is independently selected from hydrogen, alkyl, substituted alkyl, or hydroxyl; m is selected from 0-5; and R⁵ is selected from H, alkyl, or halo.

In another embodiment, with respect to compounds of formulae XIIa-XIIj, Cy is cyclohexyl; m is 1 and R^(4a) is hydroxy.

In another embodiment, with respect to compounds of formulae XIIa-XIIj, m is 1 and R^(4a) is hydroxy.

In another embodiment, with respect to compounds of formulae XIIa-XIIj, m is 1-4 and R^(4a) is methyl.

In another embodiment, with respect to compounds of formulae XIIa-XIIj, m is 1-4 and R^(4a) is methyl.

In one embodiment, with respect to compounds of formulae I-X, each of W and Z is independently CR⁴.

In one embodiment, with respect to compounds of formulae I-X, each of W and Z is independently CH.

In one embodiment, with respect to compounds of formulae I-X, W is N.

In one embodiment, with respect to compounds of formulae I-X, W is N and Z is H.

In one embodiment, with respect to compounds of formulae II-XIIj, R⁵ is H.

In one embodiment, with respect to compounds of formulae II-XXIIj, R⁵ is selected from alkyl, cycloalkyl, substituted alkyl and halo. In one particular embodiment, R⁵ is selected from Me, cyclopropyl, Cl, F and CF₃.

In one embodiment, with respect to compounds of formulae II-XIIj, R⁵ is Me.

In one embodiment, with respect to compounds of formulae II-XIIj, R⁵ is CF₃.

In one embodiment, with respect to compounds of formulae II-XIIj, R⁵ is F.

In a further embodiment with respect to compounds of formulae II-XIIj, R⁵ is Cl.

In a further embodiment with respect to compounds of formulae II-XIIId, R⁵ is cyclopropyl.

In certain aspects, the present invention provides prodrugs and derivatives of the compounds according to the formulae above. Prodrugs are derivatives of the compounds of the invention, which have metabolically, cleavable groups and become by solvolysis or under physiological conditions the compounds of the invention, which are pharmaceutically active, in vivo. Such examples include, but are not limited to, choline ester derivatives and the like, N-alkylmorpholine esters and the like.

Other derivatives of the compounds of this invention have activity in both their acid and acid derivative forms, but the acid sensitive form often offers advantages of solubility, tissue compatibility, or delayed release in the mammalian organism (see, Bundgard, H., Design of Prodrugs, pp. 7-9, 21-24, Elsevier, Amsterdam 1985). Prodrugs include acid derivatives well know to practitioners of the art, such as, for example, esters prepared by reaction of the parent acid with a suitable alcohol, or amides prepared by reaction of the parent acid compound with a substituted or unsubstituted amine, or acid anhydrides, or mixed anhydrides. Simple aliphatic or aromatic esters, amides and anhydrides derived from acidic groups pendant on the compounds of this invention are preferred prodrugs. In some cases it is desirable to prepare double ester type prodrugs such as (acyloxy)alkyl esters or ((alkoxycarbonyl)oxy)alkylesters. Preferred are the C₁ to C₈ alkyl, C₂-C₈ alkenyl, aryl, C₇-C₁₂ substituted aryl, and C₇-C₁₂ arylalkyl esters of the compounds of the invention.

Pharmaceutical Compositions

When employed as pharmaceuticals, the compounds of this invention are typically administered in the form of a pharmaceutical composition. Such compositions can be prepared in a manner well known in the pharmaceutical art and comprise at least one active compound.

Generally, the compounds of this invention are administered in a pharmaceutically effective amount. The amount of the compound actually administered will typically be determined by a physician, in the light of the relevant circumstances, including the condition to be treated, the chosen route of administration, the actual compound—administered, the age, weight, and response of the individual patient, the severity of the patient's symptoms, and the like.

The pharmaceutical compositions of this invention can be administered by a variety of routes including oral, rectal, transdermal, subcutaneous, intravenous, intramuscular, and intranasal. Depending on the intended route of delivery, the compounds of this invention are preferably formulated as either injectable or oral compositions or as salves, as lotions or as patches all for transdermal administration.

The compositions for oral administration can take the form of bulk liquid solutions or suspensions, or bulk powders. More commonly, however, the compositions are presented in unit dosage forms to facilitate accurate dosing. The term “unit dosage forms” refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient. Typical unit dosage forms include prefilled, premeasured ampules or syringes of the liquid compositions or pills, tablets, capsules or the like in the case of solid compositions. In such compositions, the furansulfonic acid compound is usually a minor component (from about 0.1 to about 50% by weight or preferably from about 1 to about 40% by weight) with the remainder being various vehicles or carriers and processing aids helpful for forming the desired dosing form.

Liquid forms suitable for oral administration may include a suitable aqueous or nonaqueous vehicle with buffers, suspending and dispensing agents, colorants, flavors and the like. Solid forms may include, for example, any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

Injectable compositions are typically based upon injectable sterile saline or phosphate-buffered saline or other injectable carriers known in the art. As before, the active compound in such compositions is typically a minor component, often being from about 0.05 to 10% by weight with the remainder being the injectable carrier and the like.

Transdermal compositions are typically formulated as a topical ointment or cream containing the active ingredient(s), generally in an amount ranging from about 0.01 to about 20% by weight, preferably from about 0.1 to about 20% by weight, preferably from about 0.1 to about 10% by weight, and more preferably from about 0.5 to about 15% by weight. When formulated as a ointment, the active ingredients will typically be combined with either a paraffinic or a water-miscible ointment base. Alternatively, the active ingredients may be formulated in a cream with, for example an oil-in-water cream base. Such transdermal formulations are well-known in the art and generally include additional ingredients to enhance the dermal penetration of stability of the active ingredients or the formulation. All such known transdermal formulations and ingredients are included within the scope of this invention.

The compounds of this invention can also be administered by a transdermal device. Accordingly, transdermal administration can be accomplished using a patch either of the reservoir or porous membrane type, or of a solid matrix variety.

The above-described components for orally administrable, injectable or topically administrable compositions are merely representative. Other materials as well as processing techniques and the like are set forth in Part 8 of Remington's Pharmaceutical Sciences 17th edition, 1985, Mack Publishing Company, Easton, Pa., which is incorporated herein by reference.

The compounds of this invention can also be administered in sustained release forms or from sustained release drug delivery systems. A description of representative sustained release materials can be found in Remington's Pharmaceutical Sciences.

The following formulation examples illustrate representative pharmaceutical compositions of this invention. The present invention, however, is not limited to the following pharmaceutical compositions.

Formulation 1—Tablets

A compound of the invention is admixed as a dry powder with a dry gelatin binder in an approximate 1:2 weight ratio. A minor amount of magnesium stearate is added as a lubricant. The mixture is formed into 240-270 mg tablets (80-90 mg of active amide compound per tablet) in a tablet press.

Formulation 2—Capsules

A compound of the invention is admixed as a dry powder with a starch diluent in an approximate 1:1 weight ratio. The mixture is filled into 250 mg capsules (125 mg of active amide compound per capsule).

Formulation 3—Liquid

A compound of the invention (125 mg), sucrose (1.75 g) and xanthan gum (4 mg) are blended, passed through a No. 10 mesh U.S. sieve, and then mixed with a previously made solution of microcrystalline cellulose and sodium carboxymethyl cellulose (11:89, 50 mg) in water. Sodium benzoate (10 mg), flavor, and color are diluted with water and added with stirring. Sufficient water is then added to produce a total volume of 5 mL.

Formulation 4—Tablets

A compound of the invention is admixed as a dry powder with a dry gelatin binder in an approximate 1:2 weight ratio. A minor amount of magnesium stearate is added as a lubricant. The mixture is formed into 450-900 mg tablets (150-300 mg of active amide compound) in a tablet press.

Formulation 5—Injection

A compound of the invention is dissolved or suspended in a buffered sterile saline injectable aqueous medium to a concentration of approximately 5 mg/ml.

Formulation 6—Topical

Stearyl alcohol (250 g) and a white petrolatum (250 g) are melted at about 75° C. and then a mixture of a compound of the invention (50 g) methylparaben (0.25 g), propylparaben (0.15 g), sodium lauryl sulfate (10 g), and propylene glycol (120 g) dissolved in water (about 370 g) is added and the resulting mixture is stirred until it congeals.

Methods of Treatment

The present compounds are used as therapeutic agents for the treatment of conditions in mammals that are causally related or attributable to aberrant activity of the P2X₇ receptor. Accordingly, the compounds and pharmaceutical compositions of this invention find use as therapeutics for preventing and/or treating autoimmune, inflammatory and cardiovascular conditions in mammals including humans.

In a method of treatment aspect, this invention provides a method of treating a mammal susceptible to or afflicted with a condition associated with arthritis, uveitis, asthma, myocardial infarction, traumatic brain injury, acute spinal cord injury, inflammatory bowel disease and autoimmune disorders, which method comprises administering an effective amount of one or more of the pharmaceutical compositions just described.

In yet another method of treatment aspect, this invention provides a method of treating a mammal susceptible to or afflicted with a condition that gives rise to pain responses or that relates to imbalances in the maintenance of basal activity of sensory nerves. The present amines have use as analgesics for the treatment of pain of various geneses or etiology, for example acute, inflammatory pain (such as pain associated with osteoarthritis and rheumatoid arthritis); various neuropathic pain syndromes (such as post-herpetic neuralgia, trigeminal neuralgia, reflex sympathetic dystrophy, diabetic neuropathy, Guillian Barre syndrome, fibromyalgia, phantom limb pain, post-masectomy pain, peripheral neuropathy, HIV neuropathy, and chemotherapy-induced and other iatrogenic neuropathies); visceral pain, (such as that associated with gastroesophageal reflex disease, irritable bowel syndrome, inflammatory bowel disease, pancreatitis, and various gynecological and urological disorders), dental pain and headache (such as migraine, cluster headache and tension headache).

In additional method of treatment aspects, this invention provides methods of treating a mammal susceptible to or afflicted with neurodegenerative diseases and disorders such as, for example Parkinson's disease, multiple sclerosis; diseases and disorders which are mediated by or result in neuroinflammation such as, for example traumatic brain injury, and encephalitis; centrally-mediated neuropsychiatric diseases and disorders such as, for example depression mania, bipolar disease, anxiety, schizophrenia, eating disorders, sleep disorders and cognition disorders; epilepsy and seizure disorders; prostate, bladder and bowel dysfunction such as, for example urinary incontinence, urinary hesitancy, rectal hypersensitivity, fecal incontinence, benign prostatic hypertrophy and inflammatory bowel disease; respiratory and airway disease and disorders such as, for example, allergic rhinitis, asthma and reactive airway disease and chronic obstructive pulmonary disease; diseases and disorders which are mediated by or result in inflammation such as, for example rheumatoid arthritis and osteoarthritis, myocardial infarction, various autoimmune diseases and disorders, uveitis and atherosclerosis; itch/pruritus such as, for example psoriasis; obesity; lipid disorders; cancer; blood pressure; spinal cord injury; and renal disorders method comprises administering an effective condition-treating or condition-preventing amount of one or more of the pharmaceutical compositions just described.

As a further aspect of the invention there is provided the present compounds for use as a pharmaceutical especially in the treatment or prevention of the aforementioned conditions and diseases. Also provided herein is the use of the present compounds in the manufacture of a medicament for the treatment or prevention of one of the aforementioned conditions and diseases.

Injection dose levels range from about 0.1 mg/kg/hour to at least 10 mg/kg/hour, all for from about 1 to about 120 hours and especially 24 to 96 hours. A preloading bolus of from about 0.1 mg/kg to about 10 mg/kg or more may also be administered to achieve adequate steady state levels. The maximum total dose is not expected to exceed about 2 g/day for a 40 to 80 kg human patient.

For the prevention and/or treatment of long-term conditions, such as neurodegenerative and autoimmune conditions, the regimen for treatment usually stretches over many months or years so oral dosing is preferred for patient convenience and tolerance. With oral dosing, one to five and especially two to four and typically three oral doses per day are representative regimens. Using these dosing patterns, each dose provides from about 0.01 to about 20 mg/kg of the compound of the invention, with preferred doses each providing from about 0.1 to about 10 mg/kg and especially about 1 to about 5 mg/kg.

Transdermal doses are generally selected to provide similar or lower blood levels than are achieved using injection doses.

When used to prevent the onset of a neurodegenerative, autoimmune or inflammatory condition, the compounds of this invention will be administered to a patient at risk for developing the condition, typically on the advice and under the supervision of a physician, at the dosage levels described above. Patients at risk for developing a particular condition generally include those that have a family history of the condition, or those who have been identified by genetic testing or screening to be particularly susceptible to developing the condition.

The compounds of this invention can be administered as the sole active agent or they can be administered in combination with other agents, including other compounds that demonstrate the same or a similar therapeutic activity, and that are determined to safe and efficacious for such combined administration.

General Synthetic Procedures

The bicycloheteroaryl compounds of this invention can be prepared from readily available starting materials using the following general methods and procedures. It will be appreciated that where typical or preferred process conditions (i.e., reaction temperatures, times, mole ratios of reactants, solvents, pressures, etc.) are given, other process conditions can also be used unless otherwise stated. Optimum reaction conditions may vary with the particular reactants or solvent used, but such conditions can be determined by one skilled in the art by routine optimization procedures.

Additionally, as will be apparent to those skilled in the art, conventional protecting groups may be necessary to prevent certain functional groups from undergoing undesired reactions. The choice of a suitable protecting group for a particular functional group as well as suitable conditions for protection and deprotection are well known in the art. For example, numerous protecting groups, and their introduction and removal, are described in T. W. Greene and P. G. M. Wuts, Protecting Groups in Organic Synthesis, Second Edition, Wiley, N.Y., 1991, and references cited therein.

The following schemes are presented with details as to the preparation of representative bicycloheteroaryls that have been listed hereinabove. The compounds of the invention may be prepared from known or commercially available starting materials and reagents by one skilled in the art of organic synthesis.

SYNTHESIS OF INTERMEDIATES Intermediate 1 Preparation of (E)-methyl 2-(2-(dimethylamino)-vinyl)-3-nitrobenzoate

A mixture of methyl 2-methyl-3-nitrobenzoate (5.0 g, 25.6 mmol) and N,N-dimethylformamide dimethyl acetal (9.18 g, 77 mmol) in DMF (30 mL) was stirred at 115° C. for 17 h. The volatiles were removed under reduced pressure to give (E)-methyl 2-(2-(dimethylamino)-vinyl)-3-nitrobenzoate as brown oil.

¹H-NMR (300 MHz, CDCl₃) δ 7.68 (m, 2H), 7.07 (t, J=7.5 Hz 1H), 6.32 (d, J=13.5 Hz, 1H), 5.65 (d, J=13.5 Hz, 1H), 73.85 (s, 3H), 2.82 (s, 6H).

Intermediate 2 Preparation of 5-Nitro-1H-isochromen-1-one

(E)-Methyl 2-(2-(dimethylamino)vinyl)-3-nitrobenzoate was re-dissolved in EtOAc (200 mL), and silica gel (200 g) was added. The resulting suspension was stirred at room temperature for 1 h. The EtOAc solution was filtered off. Silica gel was washed with EtOAc (2×150 mL) and the combined organics were evaporated and dried under reduced pressure to yield 5-nitro-1H-isochromen-1-one (4.0 g, 21.0 mmol, 82% after two steps) of as a brown solid.

¹H-NMR (300 MHz, CDCl₃) δ 8.62 (d, J=7.8 Hz, 1H), 8.47 (d, J=8.1 Hz, 1H), 7.65 (m, 1H), 7.42 (d, J=6.3 Hz, 1H), 7.36 (d, J=6.3 Hz, 1H). HPLC ret. time 1.72 min, 10-100% CH₃CN, 3.5 min gradient; ESI-MS m/z 192.1 (M+H)⁺.

Additional information can be found in McDonald, M. C. et al. British J. Pharmacol. 2000, 130, 843, incorporated herein by reference.

Intermediate 3 Preparation of 5-Amino-1H-isochromen-1-one

Tin(II) chloride dihydrate (41.9 g, 185.7 mmol) was added to a stirred solution of 5-nitro-1H-isochromen-1-one (7.1 g, 37.1 mmol) in anhydrous THF (120 mL). The reaction mixture was stirred at room temperature for 18 h. The resulting mixture was diluted with EtOAc (400 mL) and treated with saturated aqueous sodium bicarbonate to pH=10. Water (100 mL) was added and the layers were separated. The aqueous phase was extracted with ethyl acetate (2×150 mL) and the combined organic fractions were dried over Na₂SO₄, filtered and evaporated to yield 5-amino-1H-isochromen-1-one (5.8 g, 36.0 mmol, 97%) as a yellow solid.

¹H-NMR (300 MHz, CD₃OD) δ 7.52 (d, J=7.8 Hz, 1H), 7.32 (d, J=5.7 Hz, 1H), 7.27 (t, J=7.8 Hz, 1H), 7.07 (d, J=7.8 Hz, 1H), 6.80 (d, J=5.7 Hz, 1H). HPLC ret. time 1.16 min, 10-100% CH₃CN, 3.5 min gradient; ESI-MS m/z 162.3 (M+H)⁺. Additional information can be found in Lee, B. S.; et al. J. Org. Chem. 2004, 69, 3319 incorporated herein by reference.

Intermediate 4 Preparation of 2-(2-Dimethylamino-ethyl)-5-nitro-2H-isoquinolin-1-one

5-Nitro-isochromen-1-one (1.0 g, 5.2 mmol) and N,N-dimethyl-1,2-ethanediamine (4 g, 40 mmol) were refluxed in methanol (40 mL) for 1.5 hours. The volatiles were removed via rotovapor and the residue was purified via flash chromatography (12 of silica gel, 0-70% EtOAc/CH₂Cl₂ gradient) gave 2-(2-Dimethylamino-ethyl)-5-nitro-2H-isoquinolin-1-one as a yellow solid (1.4 g, 2.4 mmol, 46%).

LC/MS (0.1% formic acid modifier) calcd. (M+1)⁺ 261.28, observed 262.2.

¹H NMR (CDCCl₃) δ 8.77 (d, J=7.4 Hz, 1H), 8.40 (d, J=8.0 Hz, 1H), 7.55 (t, J=8.0 Hz, 1H), 7.34-7.28 (m, 2H), 4.12 (t, J=6.4 Hz, 2H), 2.68 (t, J=6.4 Hz, 2H), 2.30 (s, 6H).

Intermediate 5 Preparation of 5-Amino-2-(2-dimethylamino-ethyl)-2H-isoquinolin-1-one

2-(2-Dimethylamino-ethyl)-5-nitro-2H-isoquinolin-1-one (0.67 g, 2.6 mmol) and dehydrate tin dichloride (2 g, 10 mml) were stirred in THF (10 mL) at room temperature for 24 hours. The volatiles were removed via rotovapor, and the residue was dissolved in CH₂Cl₂ (1 L), washed with aqueous saturated NaHCO₃ solution (30 mL×3). The organic layer was dried over Na₂SO₄, filtered and concentrated to dryness gave 5-Amino-2-(2-dimethylamino-ethyl)-2H-isoquinolin-1-one as a yellow solid. The compound was used for next steps without further purification.

¹H NMR (CDCCl₃) δ 7.88 (d, J=8.0 Hz, 1H), 7.27 (t, J=7.9 Hz, 1H), 7.08 (d, J=7.6 Hz, 1H), 6.93 (d, J=7.7 Hz, 1H), 6.41 (d, J=7.2 Hz, 1H), 4.08 (t, J=6.7 Hz, 2H), 2.66 (t, J=6.7 Hz, 2H), 2.29 (s, 6H).

Intermediate 6 Preparation of 2-Adamantan-1-yl-N-(1-oxo-1H-isochromen-5-yl)-acetamide

To a solution of 5-amino-1H-isochromen-1-one (2.95 g, 18.3 mmol) and NMM (2.02 mL, 18.3 mmol) in 1,4-dioxane (55 mL) is added dropwise at room temperature a solution of 1-methylphenethyl acid chloride (18.3 mmol) in 1,4-dioxane (40 mL). The reaction mixture is stirred at room temperature for 3 h and then is partitioned between DCM (400 mL) and water (200 mL). The layers are separated. The aqueous phase is washed with DCM (100 mL). The combined organic layers are dried over sodium sulfate, filtered and evaporated to yield the crude N-(1-oxo-1H-isochromen-5-yl)-acetamide derivative.

Preparation of N-[2-(2-Dimethylamino-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-3-p-tolyl-propionamide)

5-Amino-2-(2-dimethylamino-ethyl)-2H-isoquinolin-1-one (50 mg, 0.2 mmol), HATU (99 mg, 0.26 mmol), 3-(4-methylphenyl)propionic acid (42 mg, 0.26 mmol) and DIPEA (110 mg, 0.86 mmol) were stirred in methylene chloride (3 mL) at room temperature for 16 hours. The mixture was purified via flash chromatography (12 g of silica gel, 0-10% MeOH/CH₂Cl₂ gradient) gave N-[2-(2-Dimethylamino-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-3-p-tolyl-propionamide as a white solid (31 mg, 0.08 mmol, 40%).

LC/MS (0.1% formic acid modifier) calcd. (M+1)⁺ 377.48, observed 378.2.

¹H NMR (CDCCl₃) δ 8.27 (d, J=8.0 Hz, 1H), 7.84 (d, J=7.6 Hz, 1H), 7.43 (t, J=7.9 Hz, 1H), 7.20-7.13 (m, 4H), 7.02 (d, J=7.6 Hz, 1H), 5.97 (d, J=7.6 Hz, 1H), 4.07 (t, J=6.5 Hz, 2H), 3.07 (t, J=7.3 Hz, 2H), 2.77 (t, J=7.3 Hz, 2H), 2.64 (t, J=6.5 Hz, 2H), 2.35 (s, 3H), 2.30 (s, 6H)

Preparation of N-[2-(2-Dimethylamino-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-2-p-tolyl-acetamide

5-Amino-2-(2-dimethylamino-ethyl)-2H-isoquinolin-1-one (50 mg, 0.2 mmol), HATU (99 mg, 0.26 mmol), p-tolylacetic acid (39 mg, 0.26 mmol) and DIPEA (110 mg, 0.86 mmol) were stirred in methylene chloride (3 mL) at room temperature for 18 hours. The mixture was purified via flash chromatography (12 g of silica gel, 0-10% MeOH/CH₂Cl₂ gradient) gave N-[2-(2-Dimethylamino-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-2-p-tolyl-acetamide as a white solid (20 mg, 0.055 mmol, 27%).

LC/MS (0.1% formic acid modifier) calcd. (M+1)⁺ 363.45, observed 364.5.

¹H NMR (CDCl₃) δ 8.24 (d, J=8.0 Hz, 1H), 8.01 (d, J=7.4 Hz, 1H), 7.46 (t, J=7.9 Hz, 1H), 7.31-7.26 (m, 4H), 7.04 (d, J=7.6 Hz, 1H), 5.93 (d, J=7.6 Hz, 1H), 4.05 (t, J=6.5 Hz, 2H), 3.81 (s, 2H), 2.63 (t, J=6.5 Hz, 2H), 2.40 (s, 3H), 2.28 (s, 6H).

Alternate Representative Method for Preparation of N-substituted-1-oxo-1,2-dihydro-isoquinolin-5-yl derivatives

The reactions were performed using 0.089 mmoles of the pyrone and a 6-fold excess of the amine. All reactions were monitored by LC/MS for completion and upon completion were purified by preparative HPLC using 0.1% formic acid buffer. The N-L¹-R³ substituted compounds of this invention, wherein L¹-R³ is as described for formula I, are or can be prepared in a manner analogous to that described in Method B1, or some modification thereof, unless otherwise described.

Representative Synthetic Methods Method A (Compound 1006) N-[2-(2-Dimethylamino-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-benzamide

a. 2-(2-Dimethylamino-ethyl)-5-nitro-2H-isoquinolin-1-one

5-Nitro-isochromen-1-one (1.83 g, 0.00957 mol) and N,N-dimethyl-1,2-ethanediamine (3 g, 0.03 mol) were refluxed in methanol (20 mL, 0.5 mol) for 1 hour. The volatiles were removed via rotovapor. The residue was purified via flash chromatography (40 g of silica gel, 50% EtOAc/CH₂Cl₂) and gave a light yellow solid.

MS m/z (M+H) 262.3.

b. 5-Amino-2-(2-dimethylamino-ethyl)-2H-isoquinolin-1-one

2-(2-Dimethylamino-ethyl)-5-nitro-2H-isoquinolin-1-one (1.10 g, 0.00358 mol) was dissolved in MeOH (30 mL), Pd/C (10%) was added and the mixture was stirred under an atmosphere of hydrogen at room temperature for 1 h. The mixture was filtered through Celite, and the solvent was removed in vacuo to give the titled product as a light yellow solid (0.82 g). MS m/z (M+H) 232.4.

c. N-[2-(2-Dimethylamino-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-benzamide

5-Amino-2-(2-dimethylamino-ethyl)-2H-isoquinolin-1-one (50 mg, 0.0002 mol), benzoyl chloride (36 mg, 0.00026 mol) and N,N-diisopropylethylamine (110 mg, 0.00086 mol) were stirred in methylene chloride (3 mL, 0.05 mol) at room temperature for 2 hours. The mixture was diluted with CH₂Cl₂ (20 mL) and the organic layer was separated and washed with NaHCO₃ (10 mL), dried over Na₂SO₄, and purified via flash column chromatography (12 g of silica gel, 10% MeOH/CH₂Cl2) to give the product as a light yellow solid.

¹H NMR δ (CDCl₃) δ: 8.34 (d, J=8.0 Hz, 1H), 8.08 (d, J=7.5 Hz, 1H), 7.96-7.92 (m, 3H), 7.66-7.52 (m, 5H), 6.53 (d, J=7.6 Hz, 1H), 4.26-4.17 (m, 2H), 3.09-3.07 (m, 2H), 2.46 (s, 6H). MS m/z (M+H) 336.4.

Method B (Compound 1013) 2-Cycloheptyl-N-[2-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-acetamide

a. 2-(2,3-Dihydro-benzo[1,4]dioxin-6-ylmethyl)-5-nitro-2H-isoquinolin-1-one

5-Nitro-isochromen-1-one (1.0 g, 0.0052 mol) and C-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-methylamine (1.0 g, 0.0060 mol) were refluxed in methanol (40 mL, 1 mol) for 2 hours. The solvent was removed and the residue was purified via flash chromatography (40 g of silica gel, 0-30% EtOAc/Hexanes) to give a yellow solid.

MS m/z (M+H) 339.5

b. 5-Amino-2-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-2H-isoquinolin-1-one

2-(2,3-Dihydro-benzo[1,4]dioxin-6-ylmethyl)-5-nitro-2H-isoquinolin-1-one (0.9 g, 0.002 mol), tin dichloride dihydrate (2 g, 0.009 mol) were stirred in tetrahydrofuran (10 mL, 0.1 mol) at room temperature for 20 hours. The volatiles were removed and the residue was purified via flash column chromatography (40 g of silica gel, 50% EtOAc/Hexanes) to give a red oil. MS m/z (M+H) 309.4.

c. 2-Cycloheptyl-N-[2-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-acetamide

5-Amino-2-(2,3-dihydro-benzo[1,4]dioxin-6-ylmethyl)-2H-isoquinolin-1-one (50 mg, 0.0002 mol), 2-cycloheptylacetic acid (63 mg, 0.00041 mol), fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (110 mg, 0.00041 mol) and N,N-diisopropylethylamine (100 mg, 0.0008 mol) were stirred in methylene chloride (3 mL, 0.05 mol) at room temperature for 72 hours. The mixture was purified via flash chromatography (12 g of silica gel, 50% EtOAc/Hexane) to give a light yellow solid.

¹H NMR δ (CDCl₃) δ: 8.33 (d, J=8.0 Hz, 1H), 7.94 (d, J=7.6 Hz, 1H), 7.47 (t, J=7.9 Hz, 1H), 7.19 (br, 1H), 7.10 (d, J=7.6 Hz, 1H), 6.82-6.78 (m, 3H), 6.42 (d, J=11.2 Hz, 1H), 5.09 (S, 2H), 4.14 (s, 4H), 2.35 (d, J=7.2 Hz, 2H), 2.20-2.13 (m, 1H), 1.85-1.26 (m, 12H).

Method C (Compound 1024) 2-Cycloheptyl-N-(2-methyl-1-oxo-1,2-dihydro-isoquinolin-5-yl)-acetamide

a. 2-Methyl-5-nitro-2H-isoquinolin-1-one

5-Nitro-isochromen-1-one (1.2 g, 0.0063 mol) and 40% aqueous methylamine (10 mL, 0.09 mol) were refluxed in methanol (40 mL, 1 mol) for 1 hour. The solvents were removed and the residue was diluted with CH₂Cl₂/MeOH (95:5 v/v, 100 mL), washed with brine (20 mL×2). The CH₂Cl₂ layer was dried over Na₂SO₄, purified via flash chromatography (40 g of silica gel, 0-50% EtOAc/Hexanes) to give a yellow solid. MS m/z (M+H) 204.8.

b. 5-Amino-2-methyl-2H-isoquinolin-1-one

2-Methyl-5-nitro-2H-isoquinolin-1-one (0.69 g, 0.0032 mol) and tin dichloride dihydrate (2 g, 0.01 mol) were stirred in tetrahydrofuran (10 mL, 0.1 mol) at room temperature overnight. The mixture was purified via flash chromatography (40 g of silica gel, 50% EtOAc/Hexanes) to give a brown solid. MS m/z (M+H) 174.9.

c. 2-Cycloheptyl-N-(2-methyl-1-oxo-1,2-dihydroisoquinolin-5-yl)acetamide

5-Amino-2-methyl-2H-isoquinolin-1-one (50 mg, 0.0003 mol), 2-cycloheptylacetic acid (90 mg, 0.0006 mol), fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (200 mg, 0.0006 mol), N,N-diisopropylethylamine (100 mg, 0.0009 mol) were stirred in methylene chloride (2 mL, 0.03 mol) at room temperature over 72 hours. The mixture was purified via flash chromatography (12 g of silica gel, 0-50% EtOAc/Hexane) to give a yellow solid. ¹H NMR δ (CDCl₃) δ: 8.31 (d, J=7.9 Hz, 1H), 7.95-7.92 (m, 1H), 7.47 (t, J=7.9 Hz, 1H), 7.20 (br, 1H), 7.11 (d, J=7.6 Hz, 1H), 6.41 (d, J=7.5 Hz, 1H), 3.60 (s, 3H), 2.37 (d, J=7.3 Hz, 2H), 2.17 (br, 1H), 1.86-1.25 (12H).

Method D (Compound 1373) 2-Cycloheptyl-N-[1-oxo-2-(tetrahydro-pyran-4-ylmethyl)-1,2-dihydro-isoquinolin-5-yl]-acetamide

a. 5-Nitro-2-(tetrahydro-pyran-4-ylmethyl)-2H-isoquinolin-1-one

5-Nitro-isochromen-1-one (1.0 g, 0.0052 mol) and C-(tetrahydro-pyran-4-yl)-methylamine (0.72 g, 0.0063 mol) were stirred in 1,4-dioxane (3 mL, 0.04 mol) at 120° C. for 18 hours. The mixture was diluted with EtOAc (200 mL), washed with 1 N HCl (30 mL×2), brine (30 mL) and dried over Na₂SO₄. After the filtration the solvent was removed and the residue was purified via flash chromatography (40 g of silica gel, 40% EtOAc/Hexanes) to give a yellow oil. MS m/z (M+H) 289.1.

b. 5-Amino-2-(tetrahydro-pyran-4-ylmethyl)-2H-isoquinolin-1-one

5-Nitro-2-(tetrahydro-pyran-4-ylmethyl)-2H-isoquinolin-1-one (0.78 g, 0.0027 mol) and tin dichloride dihydrate (2 g, 0.01 mol) were stirred in tetrahydrofuran (10 mL, 0.1 mol) at room temperature for 24 hours. The mixture was partitioned between EtOAc (100 mL) and saturated aqueous NaHCO₃ solution, separated. The aqueous layer was extracted with EtOAc (50 mL×3). The combined organic layers were dried over Na₂SO₄, and purified via flash chromatography (40 g of silica gel, 0-100% EtOAc/Hexanes) to give a yellow solid. MS m/z (M+H) 259.2.

c. 2-Cycloheptyl-N-[1-oxo-2-(tetrahydro-pyran-4-ylmethyl)-1,2-dihydro-iso quinolin-5-yl]-acetamide

5-Amino-2-(tetrahydro-pyran-4-ylmethyl)-2H-isoquinolin-1-one (40 mg, 0.0002 mot), 2-cycloheptylacetic acid (63 mg, 0.00041 mol), fluoro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (110 mg, 0.00041 mol), N,N-diisopropylethylamine (100 mg, 0.0008 mol) were stirred in methylene chloride (3 mL, 0.05 mol) at room temperature over 72 hours. The mixture was purified via flash chromatography (12 g of silica gel, 0-50% EtOAc/Hexane) to give a light yellow solid.

¹H NMR δ (CDCl₃) δ: 8.31 (d, J=6.9 Hz, 1H), 7.94 (d, J=8.2, 1H), 7.49 (t, J=8.1 Hz, 1H), 7.14 (br, 1H), 7.06 (d, J=7.5 Hz, 1H), 6.41 (d, J=7.1 Hz, 1H), 3.99-3.95 (m, 2H), 3.87 (d, J=7.3 Hz, 2H), 3.37-3.32 (m, 2H), 2.98-2.92 (m, 2H), 2.39-2.37 (m, 2H), 1.98-1.15 (m, 16H).

Method E (Compound 1380) Acetic acid 2-{5-[2-(4-chloro-3-trifluoromethyl-phenyl)-acetylamino]-1-oxo-1H-isoquinolin-2-yl}-ethyl ester

a. 2-(2-hydroxyethyl)-5-nitrosoquinolin-1(2H)-one

5-Nitro-isochromen-1-one (3.60 g, 0.0170 mol) was suspended in methanol (40 mL), ethanolamine (3.11 g, 0.0508 mol) was added and the reaction mixture was stirred at 70° C. for 2 h under an atmosphere of nitrogen. The mixture was cooled to room temperature and triethylamine (5 mL) was added. The reaction mixture was stirred at room temperature over weekend (2 days). Solid thus formed was filtered out (yellow solid was obtained as the desired product, 0.9 g). Filtrate was concentrated and the residue was dissolved in ethyl acetate, washed with water and brine, dried over sodium sulfate, solvent was removed to give the product as a yellow solid (1.3 g).

b. 2-(5-Nitro-1-oxoisoquinolin-2(1H)-yl)ethyl acetate

2-(2-Hydroxyethyl)-5-nitroisoquinolin-1(2H)-one (2.2 g, 0.0089 mol) was dissolved in the mixture of dichloromethane (20 mL) and dimethylformamide (10 mL), N,N-diisopropylethylamine (2.33 mL, 0.0134 mol) and acetyl chloride (1.06 g, 0.0134 mol) were added and the reaction mixture was stirred at room temperature for 30 min. The volatiles were removed, the residue was washed with water and then with diethyl ether to obtain a light yellow solid (2.45 g). MS m/z=276.5 (M+H).

c. 2-(5-Amino-1-oxoisoquinolin-2(1H)-yl)ethyl acetate

A mixture of 2-(5-Nitro-1-oxoisoquinolin-2(1H)-yl)ethyl acetate (2.45 g, 0.00842 mol) was dissolved in methanol (100 mL), palladium on charcoal (10%) was stirred under an atmosphere of hydrogen for 1 hour. The mixture was filtered through celite, solvent was removed to obtain the product as a light orange solid (1.98 g). MS m/z=248.0 (M+H).

d. Acetic acid 2-5-[2-(4-chloro-3-trifluoromethyl-phenyl)-acetylamino]-1-oxo-1#H!-isoquinolin-2-yl-ethyl ester

A solution of 2-(4-chloro-3-(trifluoromethyl)phenyl)acetic acid (131 mg, 0.000548 mol) in thionyl chloride (5 mL) was stirred at 60° C. for 1 hour. Thionyl chloride was removed and the residue was dissolved in tetrahydrofuran (5 mL). 245-Amino-1-oxoisoquinolin-2(1H)-yl)ethyl acetate (100.0 mg, 0.0003655 mol) and N,N-diisopropylethylamine (95.5 uL, 0.000548 mol) were added to the THF solution and the reaction mixture was stirred at room temperature for 1 h. The volatiles were removed, residue was dissolved in ethylacetate, washed with water, 2N HCl and brine. The combined organic layers were dried over sodium sulfate and the solvent removed. The residue purified by column to obtain the product as a beige solid (65 mg). MS m/z=467.0 (M+H).

¹H NMR (400 MHz, DMSO-d₆) δ: 10.11 (s, 1H), 8.07 (d, J=7.71 Hz, 1H), 7.89 (s, 1H), 7.84 (d, J=7.71 Hz, 1H), 7.73-7.68 (m, 2H), 7.51-7.45 (m, 2H), 6.68 (d, J=7.71 Hz, 1H), 4.33 (t, J=5.46, 2H), 4.20 (t, J=5.46 Hz, 2H), 3.92 (s, 2H), 1.95 (s, 3H).

Method F (Compound 1623) 2-(4-Chloro-3-trifluoromethyl-phenyl)-N-[2-(2-methoxy-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]-acetamide

a. 2-2-methoxyethyl)-5-nitroisoquinolin-1(2H)-one

Into a round bottom flask was combined 5-nitro-isochromen-1-one (5.00 g, 0.0235 mol), 2-Methoxyethylamine (6.14 mL, 0.0706 mol) and methanol (150 mL, 3.7 mol). The mixture was heated at reflux for 1.5 hours. The mixture was cooled to room temperature and triethylamine (6.56 mL, 0.0471 mol) was added. The mixture was stirred at room temperature overnight. LC-MS showed the starting material was completely consumed. Excess triethylamine and ethyl acetate was added and the mixture was stirred at room temperature for 30 mins. A yellow precipitate was formed which was filtered and the filtrate was concentrated to yield a yellow solid. The combined solids were taken onto the next step without further purification.

b. 5-Amino-2-(2-methoxyethyl)isoquinolin-1(2H)-one

Into a 250 ml round bottom flask was combined 2-(2-methoxyethyl)-5-nitroisoquinolin-1(2H)-one (1.23 g, 0.00495 mol) palladium/C (0.05 g, 0.0005 mol) and methanol (50 mL, 1 mol). The flask was purged and evacuated with hydrogen twice and the mixture was allowed to stirr under an atmosphere of hydrogen (1 atm) for two hours. The mixture was filtered over Celite and the filtrate reduced in vacuo to yield the title compound as a light brown solid.

c. 2-(4-Chloro-3-(trifluoromethyl)phenyl)-N-(1,2-dihydro-2-(2-methoxyethyl)-1-oxoisoquinolin-5-yl)acetamide

Into a 20 ml reaction vial was combined 5-amino-2-(2-methoxyethyl)isoquinolin-1(2H)-one (0.020 g, 0.000087 mol) 2-(4-chloro-3-(trifluoromethyl)phenyl)acetic acid (31 mg, 0.00013 mol) N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (81.66 mg, 0.0002148 mol) N,N-diisopropylethylamine (69.2 uL, 0.000397 mol) and N,N-dimethylformamide (1 mL, 0.02 mol). The mixture was heated at 40 degrees for 12 hours. The reaction was allowed to cool and was poured into sat sodium bicarbonate (200 ml). The mixture was extracted with ethyl acetate (3×100 ml). The combined extracts were dried over sodium sulfate and reduced in vacuo. The remaining residue was purified by reversed phase prep HPLC using acetonitrile: water gradient at pH 10. The combined pure fractions were reduced in vacuo to yield the compound as an off white solid. LC_MS (M+H)=439.2.

Method G (Compound 1624) 2-(4-Chloro-3-trifluoromethyl-phenyl)-N-[1-oxo-2-(6-trifluoromethyl-pyridin-3-ylmethyl)-1,2-dihydro-isoquinolin-5-yl]-acetamide

a. 2((6(Trifluoromethyl)pyridin-3-yl)methyl)-5-nitroisoquinolin-1(2H)-one

C-(6-Trifluoromethyl-pyridin-3-yl)-methylamine (1.00 g, 0.00568 mol) and 5-nitro-isochromen-1-one (1.14 g, 0.00568 mol) were suspended in methanol (10 mL) and the suspension was stirred at 60° C. for 3 hours, then the reaction was microwaved at 100 watts at 100° C. for 60 minutes, and then at 120° C. for 30 min. Solid thus formed was filtered out to yield the product as a yellow solid (1.2 g). MS m/z=350.4 (M+H).

b. 5-Amino-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)isoquinolin-1(2H)-one

Palladium on charcoal (10%) was added to the solution of 2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5-nitroisoquinolin-1(2H)-one (1.16 g, 0.00315 mol) in methanol (30 mL) and the mixture was stirred under an atmosphere of hydrogen for 40 min. The mixture was filtered through celite. The filterate was concentrated and the residue was purified by column to obtain the product as a beige solid (0.83 g). MS m/z=320.3 (M+H).

c. 2-(4-Chloro-3-(trifluoromethyl)phenyl)-N-(2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-1,2-dihydro-1-oxoisoquinolin-5-yl)acetamide

2-(4-Chloro-3-(trifluoromethyl)phenyl)acetic acid (142 mg, 0.000595 mol) was dissolved in thionyl chloride (10 mL) and the mixture was stirred at 60° C. for 3 hours. The volatiles were removed and the residue was dissolved in tetrahydrofuran. 5-Amino-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)isoquinolin-1(2H)-one (100.0 mg, 0.0002975 mol) and N,N-diisopropylethylamine (0.104 mL, 0.000595 mol) were added and the mixture was stirred for 1 hour at room temperature. Methanol was added to quench the reaction and the volatiles were removed. The residue was dissolved in ethylacetate, washed with water, sodium carbonate solution and brine and purified by column to obtain the product as a beige solid (120 mg). MS m/z=540.4(M+H).

1H NMR (400 MHz, DMSO-d6): 10.14 (s, 1H), 8.81 (s, 1H), 8.08 (d, J=7.89 Hz, 1H), 7.96 (d, J=8.11 Hz, 1H), 7.89-7.85 (m, 2H), 7.76 (d, J=7.57 Hz, 1H), 7.71 (s, 2H), 7.49 (t, J=8.03 Hz, 1H), 6.77 (d, J=7.83 Hz, 1H), 5.32 (s, 2H), 3.93 (s, 2H).

Method H (Compound 1628) 2-(4-Chloro-3-trifluoromethyl-phenyl)-N-(1-oxo-2-pyridin-2-ylmethyl-1,2-dihydro-isoquinolin-5-yl)-acetamide

a. 5-nitro-2-(pyridin-2-ylmethyl)isoquinolin-1(2H)-one

Into a microwave vial was combined 5-nitro-isochromen-1-one (1 g, 0.005 mol), 2-pyridinemethanamine (1 g, 0.009 mol), and methanol (20 mL, 0.5 mol). The mixture was heated at 150° C. for 2 hours. The mixture was cooled to room temperature. The usual work up of the reaction mixture gave a crude product which was then purified using a flash chromatography over silica gel to give the pure product as a yellow solid (0.7 g). MS m/z=282.4 (M+1).

b. 5-Amino-2-(pyridin-2-ylmethyl)isoquinolin-1(2H)-one

Into a round bottom flask was combined 5-nitro-2-(pyridin-2-ylmethyl)isoquinolin-1(2H)-one (0.7 g, 0.002 mol), palladium/C (0.05 g, 0.0005 mol) and methanol (200 mL, 5 mol). The reaction mixture was stirred under hydrogen balloon at room temperature for 40 mins. The mixture was filtered over celite, MeOH was removed and the solid was yield (0.46 mg). MS m/z=252.4 (M+1). 1H NMR (DMSO) δ 8.49 (d, J=4.3 Hz, 1H), 7.74 (td, J=7.7, 1.6 Hz, 1H), 7.42 (t, J=7.3 Hz, 2H), 7.27 (dd, J=6.9, 5.0 Hz, 1H), 7.22-7.12 (m, 2H), 6.88 (d, J=7.2 Hz, 1H), 6.80 (d, J=7.6 Hz, 1H), 5.69 (s, 2H), 5.23 (s, 2H).

c. 2-(4-Chloro-3-(trifluoromethyl)phenyl)-N-(1-oxo-2-(pyridin-2-ylmethyl)-1,2-dihydroisoquinolin-5-yl)acetamide

To a solution of 5-amino-2-(pyridin-2-ylmethyl)isoquinolin-1(2H)-one (100.00 mg, 0.4 mmol) in N,N-dimethylformamide (0.7 mL, 0.009 mol) was added 2-(4-chloro-3-(trifluoromethyl)phenyl)acetic acid (190 mg, 0.000796 mol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (303 mg, 0.000796 mol) and N,N-diisopropylethylamine (277 uL, 0.00159 mol). The reaction mixture was stirred for 16 hours at 50° C. Checked LC/MS, the reaction was completed. The DMF reaction solution was directly applied to prep. HPLC to obtain the pure product (134.2 mg). MS m/z=472.3 (M+1). ¹H NMR (DMSO) δ 10.13 (s, 1 H), 8.48 (d, J=4.8 Hz, 1 H), 8.06 (d, J=7/9 Hz, 1 H), 7.90 (s, 1 H), 7.84 (d, J=7.1 Hz, 1 H), 7.76 (td, J=7.7, 1.8 Hz, 1 H), 7.75-7.68 (m, 2 H), 7.63 (d, J=7.7 Hz, 1 H), 7.47 (t, J=7.9 Hz, 1 H), 7.32-7.22 (m, 2 H), 6.73 (d, J=7.6 Hz, 1 H), 5.28 (s, 2 H), 3.93 (s, 2 H).

Method J (Compound 1630) 2-(4-Chloro-3-trifluoromethyl-phenyl)-N-[2-(2-methanesulfonyl-ethyl)-1-oxo-1,2-dihydro-isoquinolin-5-yl]acetamide

a. 2-(2-(Methylsulfonyl)ethyl)-5-nitroisoquinolin-1(2H)-one

Into a round bottom flask was combined 5-nitro-isochromen-1-one (1.5 g, 0.0071 mol), 2-(methylsulfonyl)ethanamine hydrochloride (2.2 g, 0.014 mol) and methanol (45 mL, 1.1 mol). The mixture was heated at reflux for 1.5 hours. The mixture was cooled to room temperature and was concentrated to yield a yellow solid. The solid was taken onto the next step without further purification.

b. 5-Amino-2-(2-(methylsulfonyl)ethyl)isoquinolin-1(2H)-one

Into a 250 ml round bottom flask was combined 2-(2-(methylsulfonyl)ethyl)-5-nitroisoquinolin-1(2H)-one (1.20 g, 0.00405 mol) Palladium/C (0.04 g, 0.0004 mol) and methanol (40 mL, 1 mol). The flask was evacuated and purged with hydrogen 3 times. The mixture was stirred at room temperature under hydrogen (1 atm) for three hours. The mixture was filtered over celite and the filtrate was reduced in vacuo. The mixture was purified by column chromatography using a Methanol:methylene chloride (0-10%) gradient. The combined pure fractions were reduced in vacuo to yield the title compound as an off white solid.

c. 2-(4-chloro-3-(trifluoromethyl)phenyl)-N-(2-(2-(methylsulfonyl)ethyl)-1-oxo-1,2-dihydroisoquinolin-5-yl)acetamide

To a solution of 5-amino-2-(2-(methylsulfonyl)ethyl)isoquinolin-1(2H)-one (30 mg, 0.0001 mol) in N,N-dimethylformamide (700 μL, 0.009 mol) was added 2-(4-chloro-3-(trifluoromethyl)phenyl)acetic acid (51 mg, 0.00021 mol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (102 mg, 0.000268 mol) and N,N-diisopropylethylamine (93 μL, 0.00054 mol). The reaction mixture was stirred for 16 hours at 50° C. LC-MS analysis showed the formation of the desired product. The mixture was taken up in saturated NaHCO₃ solution and washed twice with ethyl acetate. The organic layer was dried with sodium sulfate, reduced in vacuo and purified via HPLC to afford the title compound as a white solid.

¹H-NMR (400 MHz, DMSO-d) δ 10.10 (s, 1H), 8.08 (d, 1H, J=7.96 Hz), 7.86 (m, 2H), 7.71 (m, 2H), 7.55 (d, 1H, J=7.73 Hz), 7.47 (t, 1H, J=7.85 Hz), 6.70 (d, 1H, J=7.73 Hz), 4.36 (t, 2H, J=6.90 Hz), 3.92 (s, 2H), 3.60 (m, 2H), 3.06 (s, 3H).

Method K (Compound 1633) 2-(2-Fluoro-3-trifluoromethyl-phenyl)-N-[1-oxo-2-(1-pyridin-2-yl-ethyl)-1,2-dihydro-isoquinolin-5-yl]-acetamide

a. 5-nitro-2(1-(pyridin-2-yl))ethyl)isoquinolin-1(2H)-one

Into a microwave vial was combined 5-nitro-isochromen-1-one (1 g, 0.005 mol), 1-pyridin-2-yl-ethylamine (1 g, 0.009 mol), and methanol (20 mL, 0.5 mol). The mixture was heated at 150° C. for 2 hours. The mixture was cooled to room temperature. LC-MS showed the starting material was completely consumed. After silica gel column, a yellow solid was obtained (0.85 g). MS m/z=295.9 (M+1).

b. 5-amino-2-(1-(pyridin-2-yl)ethyl)isoquinolin-1(2H)-one

Into a round bottom flask was combined 5-nitro-2-(1-(pyridin-2-yl)ethyl)isoquinolin-1(2H)-one (0.85 g, 0.0029 mol), Palladium/C (0.05 g, 0.0005 mol) and methanol (200 mL, 5 mol). The reaction mixture was stirred under hydrogen balloon at room temperature for 40 mins. The mixture was filtered over celite, MeOH was removed and the solid was yield (0.54 mg). MS m/z=266.0 (M+1). ¹H NMR (DMSO) δ 8.55 (d, J=4.8 Hz, 1 H), 7.77 (td, J=7.7, 1.8 Hz, 1 H); 7.44 (d, J=7.8 Hz, 1 H), 7.35-7.25 (m, 3 H), 7.17 (t, J=7.8 Hz, 1 H), 6.95-6.85 (m, 1 H), 6.78 (d, J=7.8 Hz, 1 H), 6.28 (q, J=7.2 Hz, 1 H), 5.66 (s, 2 H), 1.75 (d, J=7.2 Hz, 3 H).

c. 2-(2-Fluoro-3-(trifluoromethyl)phenyl)-N-(1-oxo-2-(1-(pyridin-2-yl)ethyl)-1,2-dihydroisoquinolin-5-yl)acetamide

To a solution of 5-amino-2-(1-(pyridin-2-yl)ethyl)isoquinolin-1(2H)-one (100 mg, 0.0004 mol) in N,N-Dimethylformamide (1 mL, 0.01 mol) was added 2-(2-fluoro-3-(trifluoromethyl)phenyl)acetic acid (178 mg, 0.000801 mol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (468.3 mg, 0.001232 mol) and N,N-diisopropylethylamine (300 uL, 0.002 mol). The reaction mixture was stirred for 16 hours at 50° C. LC/MS indicated that the reaction was completed. The DMF reaction solution was directly applied to prep. HPLC. The final product was obtained as a solid (102.4 mg). MS m/z=470.3 (M+1). ¹H NMR (DMSO) δ 10.17 (s, 1 H), 8.54 (d, J=6.4 Hz, 1 H), 8.10 (d, J=8.0 Hz, 1 H), 7.82 (dd, J=7.8, 0.7 Hz, 1 H), 7.78 (td, J=9.5, 1.8 Hz, 2 H), 7.70 (t, J=7.1 Hz, 1 H), 7.55 (d, J=7.8 Hz, 1 H), 7.48 (t, J=7.9 Hz, 1 H), 7.40 (t, J=7.7 Hz, 1 H), 7.35 (d, J=8.0 Hz, 1 H), 7.31 (qd, J=4.8, 0.9 Hz, 1 H), 6.74 (d, J=7.8 Hz, 1 H), 6.28 (q, J=7.2 Hz, 1 H), 3.98 (s, 2 H), 1.78 (d, J=7.2 Hz, 3 H).

EXAMPLE 1

The P2X₇ receptor is strongly expressed in macrophage-derived cell lines, including, but not limited to, J774 (mouse macrophage line, American Type Culture Collection (ATCC), Rockville, Md., ATCC TIB-67), P388 (mouse cell line, ATCC CCL-46), P815 (mouse mast cell mastocytoma-derived line, ATCC TIB-64), THP-1 (Human monocyte-derived cell line, ATCC TIB202) and U937 (human cell line derived from histiocytic lymphoma, induceable to monocyte differentiation, ATCC CRL-1593.2) and in isolated macrophage cultures. Human or non-human animal macrophages are isolated using the procedure noted below.

The P2Z/P2X₇ receptor can be characterized by measuring channel opening, for instance ion flux, and/or by assessing pore formation, including by monitoring dye uptake or cell lysis in cells naturally expressing this receptor. Compounds such as ATP, 2′ and 3′-(O)-(4-benzoyl benzoyl) ATP (BzATP) effect the formation of pores in the plasma membrane of these cells, particularly at low extracellular divalent ion concentrations (Buisman et al, Proc. Natl. Acad. Sci. USA 85:7988 (1988); Zambon et al, Cell. Immunol 156:458 (1994); Hickman et al Blood 84:2452 (1994)). Large molecular size dyes, including propidium dye YO-PRO-1, can be seen entering macrophage-derived cell lines during cell recordings (Hickman et al, Blood 84:2452 (1994); Wiley et al, Br J Pharmacol 112:946 (1994); Steinberg et al, J Biol Chem 262:8884 (1987)). Ethidium bromide (a fluorescent DNA probe) can also be monitored, where an increase in the fluorescence of intracellular DNA-bound ethidium bromide is observed. Expression of recombinant rat or human rP2X₇ in cells, including HEK293 cells, and in Xenopus oocytes demonstrates influx and pore formation by whole cell recordings and YO-PRO-1 fluorescence (Suprenant et al, Science 272:735 (1996); Rassendren et al, J Biol Chem 272:5482 (1997)).

The compounds of the invention may be tested for antagonist activity at the P2X₇ receptor. Tests to be performed include and are selected from: (i) electrophysiological experiments; (ii) YO-PRO1 fluorescence; (iii) ethidium bromide fluorescence; and (iv) IL-1β release from stimulated macrophages, including as described below. Compounds can be tested in vivo in animal models including for inflammation models (e.g. paw edema model, collagen-induced arthritis, EAE model of MS).

Isolation of Human Macrophages

Monocyte-derived human or non-human animal macrophage cultures are prepared as described by Blanchard et al (Blanchard et al, J Cell Biochem 57:452 (1995); Blanchard et al, J Immunol 147:2579 (1991)). Briefly, monocytes are isolated from leukocyte concentrates obtained from a healthy volunteer. Leukocytes are suspended in RPMI 1460 medium (Life Techologies, Inc.) with 20% serum (human for human cells), 2 mM glutamine, 5 mM HEPES, and 100 μg/ml streptomycin. Cells are allowed to adhere to culture flasks for 1-2 h, after which nonadherent cells are washed away. Adherent cells are cultured for 7-14d in this medium plus interferon-γ (human for human cells) (1000 units/ml). Macrophages are recovered from the culture flask by pipetting with cold phosphate-buffered saline and plated onto glass coverslips for electrophysiological or other experiments carried out 12-24 h later.

EXAMPLE 2 Electrophysiological Experiments

Whole cell recordings are made using the EPC9 patch-clamp amplifier and Pulse acquisition programs (HEKA, Lambrecht, Germany). Whole-cell recordings are obtained from cells, e.g. J774A.1 cells (American Type Culture Collection, Rockville, Md., ATCC TIB-67)); agonists are applied for periods of 1 to 3 s by a fast-flow U-tube delivery system [E. M. Fenwick, A. Marty, E. Neher, J. Physiol, (London) 331, 577 (1982)]. The internal pipette solution is 140 mM cesium-aspartate or potassium-aspartate, 20 mM NaCl, 10 mM EGTA, and 5 mM Hepes; normal external solution is 145 mM NaCl, 2 mM KCl, 2 mM CaCl₂, 1 mM MgCl₂, 10 mM Hepes, and 12 mM glucose. Low divalent external solution is nominally magnesium-free with 0.3 mM CaCl₂. Concentration-response curves are constructed in low divalent solution by recording currents in response to 1 s applications of agonist at 8 min intervals with normal external solution present for 6 min before each application. This protocol is necessary to prevent the development of sustained inward currents.

Reversal potentials (E_(rev)) are obtained by application of ATP (300 μM) or BzATP (30 μM)(controls), or the compound being tested, while the membrane is held at various potentials or by application of voltage ramps from −120 to 30 or 50 mV. Permeability ratios are calculated from E_(rev), by first computing α(=P_(Na)/P_(K′) where P is permeability) for internal (i) and external (o) concentrations [Na]_(i)=20 mM, [Na]_(o)=145 mM, [K]_(o)=0 mM, and [K]_(i)=140 mM from α=([145/exp(E_(rev)FIRT)]−20)/140 (where F is the Faraday, R is the gas constant, and T is the absolute temperature). Other P_(x)/P_(Na) values, when [X]_(o)=145 mM, [Na]_(i)=20 mM, [K]_(i)=140 mM, and [Na]_(o)=[K]_(o)=[X]_(i)=0 mM, are computed from P_(x)/P_(Na)=[(exp)E_(rev)F/RT)] (20+140α))/145. In order of size, X is cesium, methylamine, tris(hydroxymethyl)-aminomethane, tetraethylammonium, and N-methyl-D-glucamine. The internal solution also contains 10 mM EGTA and 5 mM Hepes. External solutions also contain 10 mM glucose and normal or low concentrations of divalent cations; pH is maintained at 7.3 with HCl, histidine, or Hepes as required, and the osmolarity of all solutions is 295 to 315.

EXAMPLE 3 YO-PRO1 Fluorescence

The Photonics Imaging (IDEA) system for microscopic fluorescence measurements (Photonics, Planegg, Germany) is used. Coverslips are placed at the stage of a Zeiss Axiovert 100 or equivalent inverted microscope and viewed under oil immersion with a 40× Fluor objective. YO-PRO-1 (10 μM; Molecular Probes, Eugene, Oreg.) is added to the superfusion fluid during electrophysiological recordings 3 to 6 min before switching to low divalent solution and washed out upon switching back to normal divalent solution, after which the fluorescent lamp is turned on and cells are examined with a fluorescein isothiocyanate filter. YO-PRO1 fluorescence is measured using 491/509 nm excitation/emission wavelengths. Images are obtained at 5-20s intervals during continuous superfusion (2 ml/min) with YO-PRO1 and varying concentrations of control ATP, BzATP or compound to be tested. For each experiment, the time course of YO-PRO1 fluorescence obtained for 10-20 individual cells and then averaged to obtain the mean fluorescence signal. Results were expressed as mean signal at 3 min for rP2X₇, and the signal at 10 min is used for P2X₇ and human macrophage cells. All experiments are carried out at room temperature.

EXAMPLE 4 Ethidium Bromide

Compounds of the invention are tested for antagonist activity at the P2X₇ receptor by monitoring Ethidium Bromide entering P2X₇ receptor-expressing cells on pore formation. The test is performed in 96-well flat bottomed microtitre plates, the wells being filled with 250 μl of test solution comprising 200 μl of a suspension of P2X₇-expressing cells (e.g. THP-1 cells, J774 cells, etc.)(2.5×10⁶ cells/ml) containing 10⁻⁴M ethidium bromide, 25 μl of a high potassium buffer solution containing 10⁻⁵M BzATP, and 25 μl of a high potassium buffer solution containing test compound. The plate is covered with a plastic sheet and incubated at 37° C. for one hour. The plate is then read in a Perkin-Elmer fluorescent plate reader, excitation 520 nm, emission 595 nm, slit widths: Ex 15 nm, EM 20 nm. For the purposes of comparison, BzATP (a P2X₇ receptor agonist) and pyridoxal 5-phosphate (a P2X₇ receptor agonist) are used separately in the test as controls. From the readings obtained, a pIC₅₀ figure is calculated for each test compound. This figure is the negative logarithm of the concentration of test compound necessary to reduce the BzATP agonist activity by 50%.

EXAMPLE 5 IL-1β Release

This Example demonstrates the testing of the compounds of this invention for efficacy as inhibitors of P2X₇-mediated release of IL-1β from human macrophages activated by the Alzheimer's beta amyloid peptide 1-42.

Cell Isolation

Monocytes are isolated from peripheral blood mononuclear cells (PBMCs) as follows. Whole blood is layered directly onto Histopak 1077-1 columns (Sigma Biochemicals) and centrifuged at 800×g for 15 minutes. The PBMC band of cells is removed to a fresh 50 ml culture tube and diluted 1:1 with wash buffer (Phosphate buffered saline, pH 7.4 containing 2 mM EDTA and 5 mg/ml BSA) followed by centrifugation at 800×g for 5 minutes. Cells are then washed by sequential resuspension of the cell pellet in wash buffer and centrifugation at 600×g for 5 minutes. The wash process is repeated until the supernatent is clear of contaminating platelets (generally, 5 to 6 washes). Monocytes are then purified from the PBMCs by negative selection using a monocyte isolation kit (Miltenyi Biotec, Inc.) that contains antibodies to non-monocytic cells, running the cells over a magnetic column to remove antibody-bound cells, and collecting the flow through volume of monocytes. Monocytes are washed once with wash buffer and seeded at 100,000 cells per well in 100 p. 1 serum-free RPMI 1640 in 96-well plates and incubated for 1 hour at 37° C. in a 5% CO₂/95% humidified tissue culture incubator. After 1 hour, the medium is replaced with 100 μl complete culture medium (RPMI 1640, 10% human serum-type AB (heat inactivated), 25 mM HEPES, 2 mM glutamine, 50 U/ml each of penicillin and streptomycin) and incubated overnight (16 hours).

Dosing Regimen

The next day, the culture medium is replaced with 100 μl fresh complete culture medium in the absence or presence of human beta amyloid 1-42 peptide (5 μM) and incubated at 37° C. in a 5% CO₂/95% humidified tissue culture incubator for 5 hours. Medium is then removed and discarded. Each well is washed once with Hanks buffered saline (HBSS) containing 1 mM CaCl₂ followed by the addition of 80 μl of HBSS/CaCl₂-inhibiting compound of the present invention (10× stock in HBSS/CaCl₂ for a final concentration of 23 nM and 206 nM) and incubated 15 minutes in the tissue culture incubator followed by the addition of either 10 μl of HBSS/CaCl₂ or 10 μl of benzoyl ATP (BzATP; 3 mM stock in HBSS/CaCl₂ for a 300 μM final concentration) and incubated for a further 30 minutes in the tissue culture incubator. Medium is then removed to new 96-well plates for storage at −70° C. until the IL-113 content was quantitated by ELISA (from R&D Systems). The cells are washed once with HBSS/CaCl₂ followed by lysing the cells with 100 μl ice cold lysis buffer (100 mM Tris, pH 7.6, 1% Triton X-100, and 1 tablet per 30 ml Complete TM protease inhibitor from Roche Biochemicals, Inc). Cell lysates are stored at −70° C. until the IL-1β is quantitated by ELISA.

EXAMPLE 6 In Vivo Animal Models

A. This Example Illustrates the Efficacy of the Compounds of this Invention in the Treatment of Multiple Sclerosis.

As described herein, experimental autoimmune encephalomyelitis (EAE) model is used to show such an efficacy. The following procedures are employed in this model.

Animals

SJL/J female mice, 8 wks. old, are obtained from Jackson Laboratories.

Antigens

Myelin Proteolipid Protein (PLP 139-151) (HSLGKWLGHPDKF) (Cat # H-2478) is obtained from BACHEM, Bioscience, Inc., 3700 Horizon Dr., King of Prussia, Pa. 19406, 1-610-239-0300 (phone), 1-610-239-0800 (fax).

Complete Freund's Adjuvant H37 Ra [1 mg/ml Mycobacterium tuberculosis H37 Ra] is obtained from Difco 1-800-521-0851 (Cat # 3114-60-5, 6×10 ml).

Mycobacterium tuberculosis is also obtained from Difco, 1-800-521-0851 (Cat # 3114-33-8, 6.times.100 mg).

Pertussis Toxin

Bordetella pertussis, (Lyophilized powder containing PBS and lactose) is obtained from List Biological Laboratories, 1-408-866-6363 (Product #180, 50 ug).

Induction of EAE in Mice

PLP139-151 peptide is dissolved in H₂O:PBS (1:1) solution to a concentration 7.5 mg/10 ml (for 75 μg PLP per group) and emulsified with an equal volume of CFA supplemented with 40 mg/10 ml heated-killed Mycobacterium tuberculosis H37Ra. Mice are injected s.c. with 0.2 ml of peptide emulsion in the abdominal flank (0.1 ml on each side). On the same day and 72 hours later, mice are injected i.v. with 100% of 35 ng and 50 ng of Bordetella pertussis toxin in saline respectively.

Clinical Assessment

-   STAGE 0: Normal -   STAGE 0.5: Partial limp tail -   STAGE 1: Complete Limp Tail -   STAGE 2: Impaired righting reflex -   STAGE 2.5: Righting reflex is delayed (Not weak enough to be stage     3). -   STAGE 3: Partial hind limb paralysis -   STAGE 3.5: One leg is completely paralyzed, and one leg is partially     paralyzed, -   STAGE 4: Complete hind limb paralysis -   STAGE 4.5: Legs are completely paralyzed and Moribund -   STAGE 5: Death due to EAE

Clinical Courses of EAE

Acute phase: First clinical episode (Day 10-18)

Remission: Phase of clinical improvement following a clinical episode; characterized by a reduction (>=one grade) in clinical score for at least two days after the peak score of acute phase or a disease relapse.

Relapse: Increase of at least one grade in clinical score for at least two days after remission has been attained.

The animals treated with the compounds of this invention generally would be expected to show improvements in clinical scores.

B. This Example Illustrates a Protocol for Determining the Efficacy of the Compounds of the Present Invention for the Treatment of Stroke Using an Animal Model.

Male Sprague Dawley rats (Charles River) weighing 280-320 g are given free access to food and water and acclimatized for a minimum of 4 days before use in experiments. All rats for use in studies are to be fasted beginning at 3:00 pm the day prior to surgery but given free access to water. Prior to surgery each rat is weighed. The rat is initially induced with 5% isoflurane (Aerrane, Fort Dodge), combined with 30% O₂, 70% N₂O for 2-5 minutes. The rat is then placed on a circulating water-heating pad and into a nose cone for spontaneous respiration of anesthetic gases. The isoflurane is reduced to 2%. A rectal probe is inserted and body temperature maintained at 36.5-37.5° C. The hair is clipped at all surgical sites and these regions will then be scrubbed with Betadine.

Surgical Procedure

A temporalis muscle probe is placed into the right temporalis muscle and “brain” temperature” is monitored. A midline neck incision is made in the upper thorax of the rat. Careful dissection, isolation and retraction of the sternomastoideus, digastricus, and sternohyoideus muscles is made to expose the right common, internal and external carotid arteries. The right common carotid artery is isolated with a 5-0 silk suture. During surgery the suture is released allowing reperfusion every 2-4 minutes. The right external carotid and superior thyroid arteries are also isolated and the superior thyroid is cauterized, while the external carotid is ligated distally with a 5-0 silk suture. Another 5-0 silk suture is loosely tied around the external carotid artery. The occipital artery is isolated, ligated and incised. The internal carotid is isolated.

With the common and external carotid arteries immobilized, an aneurysm clip is placed onto the internal carotid artery. A small incision is made at the distal end of the external carotid. A 3-0 nylon suture coated with poly-L-lysine is then inserted into the external carotid and up into the common carotid artery. The loosely tied 5-0 silk suture around the external carotid is now gently tightened around the filament. The external carotid artery is then incised and the remaining piece of the external carotid artery with the filament is rotated so that the filament may be inserted into the internal carotid artery the length of insertion depending on the weight and rat strain. In Sprague Dawley rats the monofilament is inserted 18-19 mm (18 mm for rats weighing <300 gm, 19 mm for rats weighing 0.300 gm) effectively blocking blood flow to the middle cerebral artery.

The external jugular vein will be cannulated with PE 50 tubing for I.V. administration of compounds. The cannula will be exteriorized at the previously shaven, scruff of the neck and sutured in place. The wound will be closed by means of suture. The right femoral artery is catheterized for blood gas and glucose determination during surgery.

Two hours after the insertion of the monofilament suture the rats are re-anesthetized with the same anesthetic combination used initially and placed back into the nose cone with the reduction of isoflurane concentration to 2%. The neck incision is reopened to expose the external carotid artery. The restoration of blood flow is accomplished by completely withdrawing the intraluminal suture from the carotid arteries. The incision is then closed with 3-0 silk in an interrupted stitch.

Compound Administration

Five groups of 15 animals are subjected to the above methodology. Compounds are infused (I.V.) at various doses (dose response) over different time periods post MCAo. A pre-determined concentration is infused over a pre-selected time period beginning at various intervals post MCAo. Vehicle-treated controls receive an infusion of normally 0.9 ml/hr. A positive control compound is run at the same time.

Neurological Tests

Prior to surgery, 2 hours following the onset of ischaemia and 24 hours after ischaemia a battery of neurological tests are performed. The postural reflex test, which is designed to examine upper body posture, when the rat is suspended by the tail above a flat surface. A normal rat will extend the entire body and both forelimbs towards the surface. Rats with an infarction will consistently flex the contralateral limb and show signs of body rotation. The rats respond to a gentle lateral push with a finger behind the shoulders. A normal rat would resist such a push, whereas a rat with an infarction will not. The elicited forelimb placing in response to visual and tactile stimuli. The animal is held by the body so that the lateral or dorsal forepaw surface is placed against a bench. This test is repeated but on this occasion obstructing the view of the rat.

Upon completion of each experiment, all animals are deeply anaesthetized with isoflurane (5%), euthanized by decapitation, and the brains removed, the extent and location of the ischaemic damage is verified histologically by means of tetrazolium chloride.

C. This Example Illustrates the Anti-Inflammatory Activity of the Compounds of this Invention Using a Model of 2,4-dinitrobenzenesulfonic Acid (DNBS) Induced Distal Colitis (a Model of Inflammatory Bowel Disease).

Test Substance and Dosing Pattern

A compound of this invention is dissolved in vehicle of 2% Tween 80 in distilled water for oral administration at a dose of 50 mg/kg or dissolved in vehicle of 2% Tween 80 and 0.9% NaCl for intraperitoneal injection at 30 mg/kg. The dose is given once daily for 7 consecutive days. Dosing volume is 10 ml/kg. DNBS was challenged 2 hours after dosing on the second day.

Animals

In these studies, male Wistar, Long Evans rats provided by animal breeding center of MDS Panlabs Taiwan, Ltd. and Balb/cByJ derived male mice (weighing 20±2 gms), provided by National Laboratory Animals Breeding Research center (NALBRC, Taiwan), may be used. Space allocation of 6 animals may be 45×23×15 cm. Animals are housed in APEC® cages (Allentown Caging, Allentown, N.J. 08501, USA) in a positive pressure isolator (NuAire®, Mode: Nu-605, airflow velocity 50±15 ft/min, HEPA Filter) and maintained in a controlled temperature (22° C.-24° C.) and humidity (60%-80%) environment with 12 hours light dark cycles for at least one week in MDS Panlabs Taiwan laboratory prior to being used. Free access to standard lab chow for rats (Fwusow Industry Co., Limited, Taiwan) and tap water is granted. All aspects of this work including housing, experimentation and disposal of animals would be performed in general accordance with the International Guiding Principles for Biomedical Research Involving Animals (CIOMS Publication No. ISBN 92 90360194, 1985).

Chemicals

DNBS is obtained from TCI, Tokyo, Japan, ethanol is from Merck, Germany and Sulfasalazine is purchased from Sigma, USA.

Equipment

Electriconic scale (Tanita, model 1140, Japan), Electriconic scale (Sartorius, R160P, Germany), Glass syringe (2 ml, Mitsuba, Japan), Rat oral needle, Hypodermic needle (25G.times.1 “TOP Corporation, Japan), Stainless Scissors (Klappenclear, Germany), Stainless Forceps (Klappenclear, Germany).

Method

Groups of 3 Wistar derived male rats weighing 180-120 gms are used. Distal colitis is induced by intra-colonic instillation of DNBS (2,4-dinitrobenzene sulfonic acid, 30 mg in 0.5 ml ethanol 30%) after which, 2 ml of air is gently injected through the cannula to ensure that the solution remains in the colon. Test substance is administered orally (PO) at a dose of 50 mg/kg or intraperitoneally (IP) at 30 mg/kg once daily for 7 consecutive days. DNBS is instillated into the distal colon of each animal 2 hours after dosing on the second day. The control group is similarly treated with vehicle alone and sulfasalazine (300 mg/kg, PO) is used as reference agent. Animals are fasted 24 hours before DNBS challenge and 24 hours after the final treatment when they are sacrificed and each colon is removed and weighed. During the experiments, presence of diarrhea is recorded daily. When the abdominal cavity is opened before removal of the colon, adhesions between the colon and other organs are noted. After weighing the colon, the extent of colonic ulceration is observed and noted as well. Colon-to-body weight ratio is then calculated for each animal according to the formula: Colon (g)/BW×100%. The “Net” increase in ratio of Vehicle-control +DNBS group relative to Vehicle-control group is used as a base value for comparison with test substance treated groups and expressed as % decrease in inflammation. A 30 percent or more (30%) decrease in “Net” colon-to-body weight ratio for each test substance treated group relative to the “Net” vehicle+DNBS treated group is considered significant.

D. This Example Illustrates the Anti-Inflammatory Activity of the Present Compounds Using a Model of Carrageenan Induced Paw Edema (a Model of Inflammation, Carrageenan).

Test Substance and Dosing Pattern

A compound of this invention is dissolved in vehicle of 2% Tween 80/0.9% NaCl and administered intraperitoneally at a dose of 30 mg/kg 30 minutes before carrageenan (1% 0.1 ml/paw) challenge. Dosing volume is 10 ml/kg.

Animals

Animals are conditioned in accordance with the procedures set forth in the previous Example.

Chemicals

Carrageenan is obtained from TCI, Japan; Pyrogen free saline is from Astar, Taiwan; and Aspirin is purchased from ICN BioMedicals, USA.

Equipment

Glass syringe (1 ml and 2 ml Mitsuba, Japan), Hypodermic needle 24Gx1″ (Top Corporation, Japan), Plethysmometer #7150 (UGO Basile, Italy), and Water cell 25 mm Diameter, #7157 (UGO Basile, Italy).

Method

Test substance (Example) is administered IP (30 mg/kg) to groups of 3 Long Evans derived male overnight fasted rats weighing 150±20 gms 30 minutes before right hind paw injection of carrageenan (0.1 ml of 1% suspension intraplantar). Hind paw edema, as a measure of inflammation, is recorded 3 hours after carrageenan administration using a plethysmometer (Ugo Basile Cat. #7150) with water cell (25 mm diameter, Cat. #7157). Reduction of hind paw edema by 30 percent or more (30%) indicated significant acute anti-inflammatory activity.

E. This Example Illustrates the Anti-Inflammatory Activity of the Present Compounds Using a Model of Balb/c Mice Subjected to Monoclonal Antibody (mAb) Type II Collagen Induced Arthritis.

Test Substance and Dosing Pattern

A compound of this invention is dissolved in vehicle of 2% Tween 80/0.9% NaCl, at doses of 50 or 30 and administered orally (50 mg/kg) or intraperitoneally at 30 mg/kg once daily for 3 consecutive days after monoclonal antibody of collagen was injected. Dosing volume is 20 ml/kg.

Animals

Animals are conditioned in accordance with the procedures set forth in the previous Example.

Chemicals

Lipopolysaccharide is obtained from Sigma, USA; Indomethacin is from Sigma, USA; Arthrogen-CIA.TM. Monoclonal Antibodies D8, F10, DI-2G and A2 are obtained from IBL, Japan; Phosphated-Buffer Saline is purchased from Sigma, USA; and Tween 80 is from Wako, Japan.

Equipment

Plethysmometer (Ugo Basile, Italy) and Water Cell (Ugo Basile, Italy).

Method

Groups of 5 Balb/cByJ mice strain, 6-8 weeks of age, are used for the induction of arthritis by monoclonal antibodies (mAbs) responding to type II collagen, plus lipopolysaccharide (LPS). The animals are administered intravenously with a combination of 4 different mabs in a total of 4 mg/mouse at day 0, and followed by intravenous 25 μg of LPS 72 hours later (day 3). From day 3, one hour after LPS administration, ML-659 at 50 mg/kg (PO) or 30 mg/kg (IP) and vehicle (2% Tween 80/0.9% NaCl, PO) as well as the positive control indomethacin, 3 mg/kg (PO) are administrated once daily for 3 consecutive days. A plethysmometer (Ugo Basile Cat #7150) with water cell (12 mm diameter) is used for the measurement of increase in volume of the two hind paws at day 0, 5, 7, 10, 14, and 17. The percent inhibition of increase in volume is calculated by the following formula: Inhibition (%): [1−(Tn−To)/(Cn−Co)]×100 Where:

-   Co (Cn): volume of day 0 (day n) in vehicle control -   To (Tn): volume of day 0 (day n) in test compound-treated group     The reduction of both of two hind paws edema by more than 30% is     considered significant.

EXAMPLE 7 Neuropathic Pain Model

This example illustrates the analgesic activity of the compounds of this invention using a Sciatic Nerve ligation model of mononeuropathic pain

Test System

Adult male Sprague Dawley (SD) rats weighing 250-300 gm (Charles River Laboratories, San Diego, Calif.) are used. The animal room is lighted artificially at a 12-hr light-dark cycle (from 7:00 A.M. to 7:00 P.M) with water and food supply ad libitum. Animals are allocated randomly into groups.

Model Induction

Sciatic nerve ligation (SNL, Seltzer's model):

Under anesthesia with pentobarbital (50 mg/kg, i.p.) and aseptic techniques, the selective nerve injury is created by tightly ligating the selective portion of the common sciatic nerve according to the method of Seltzer (1990). Briefly, the high-thigh level of the left sciatic nerve is exposed after skin incision and blunt separation of muscles at a site near the trochanter just distal to the point at which the posterior biceps semitendious nerve nerve branches from the common sciatic nerve. The nerve is then fixed in this position with fine forceps by pinching the epineurium on its dorsal aspect, taking care not to press the nerve against underlying structures. An 8-0 silicon-treated silk suture is inserted into the nerve with a ⅜ curved, reversed-cutting mini-needle, and tightly ligated so that the dorsal ⅓-½ of the nerve is trapped in the ligature. The muscles are sutured in layers, and the skin closed with wound clips. Animals are then returned to their home cages. Rats exhibiting postoperative neurological deficits or poor grooming are excluded from the experiments. Equipment

The following equipment is used in the current studies: von Frey filament set (Touch-test Sensory Evaluator, North Coast Medical Inc., Morgan Hill, Calif.).

Statistical Methods:

Within each experiment mean, standard error of the mean (SEM) and statistical significance are calculated using the average, standard error of the mean and unpaired, two-tailed t-Test functions, respectively, using Microsoft Excel®. Statistical significance of effects observed between individual experiments is determined, using Prism (GraphPad Software Inc., San Diego, Calif.) for the one-way or two-way analysis of variance (ANOVA) function. Statistical analyses are performed with a confidence limit of 0.95 and a significance level of 0.05.

EXAMPLE 8 Pore Formation

THP-1 cells (ATCC Cat # 2854F-100) are plated in 96 well plates at a concentration of 200,000 cells per well and allowed to differentiate in RPMI-1640 media (ATCC Cat # 30-2001) containing 10% FBS, 100 IU/mL penicillin, 100 ug/mL streptomycin, 100 ng/mL LPS and 100 ng/mL IFN-γ for 16 hours. Following differentiation, the cells are pretreated with the compound of interest at the appropriate concentration for 30 minutes in RPMI-1640 media containing 100 IU/mL penicillin, 100 ug/mL streptomycin. The pretreatment media is then replaced with assay buffer (20 mM HEPES, 10 mM d-glucose, 118 mM NMDG, 5 mM KCl, 0.4 mM CaCl₂) containing 5 uM Yo-Pro 1. (Molecular Probes Cat # Y3603) and the compound of interest at the appropriate concentration and the cells are incubated for an additional 10 minutes. 2′,3′-O-(4-benzoylbenzoyl)-adenosine 5′-triphosphate (Sigma Aldrich Cat# B6396) is then added to a final concentration of 40 uM and fluoroscence readings measured at 491/509 excitation/emission every minute for 50 minutes using a Tecan Safire plate reader. During this time temperature is maintained at of 37° C. Background adjusted fluorescence levels between drug treated and non-treated cells are used to calculate the percent inhibition.

EXAMPLE 9 IL-1β Release Assay

THP-1 cells (ATCC Cat # 285-IF-100) are plated in 96 well plates at a concentration of 200,000 cells per well and allowed to differentiate in RPMI-1640 media (ATCC Cat # 30-2001) containing 10% FBS, 100 IU/mL penicillin, 100 ug/mL streptomycin, 100 ng/mL LPS and 100 ng/mL IFN-γ for 16 hours. Following differentiation, the cells are treated for an additional 2 hours in RPMI-1640 media containing 100 IU/mL penicillin, 100 ug/mL streptomycin and fresh LPS at 100 ng/mL. The cells are then pretreated for 30 minutes with the compound of interest at the appropriate concentration in RPMI media containing 100 IU/mL penicillin, 100 ug/mL streptomycin. Following the pretreatment 2′,3′-O-(4-benzoylbenzoyl)-adenosine 5′-triphosphate (Sigma Aldrich Cat # B6396) is added to a final concentration of 250 uM and the cells are incubated for an additional 45 minutes. 30 uL of cell supernatant is then collected and IL-1β levels determined via ELISA (R&D systems Cat. # HSLB50) according to manufacturer's recommendations using the Tecan Safire plate reader. Background adjusted IL-1β levels of drug treated and non-treated cells are used to calculate the percent inhibition.

The synthetic and biological examples described in this application are offered to illustrate this invention and are not to be construed in any way as limiting the scope of this invention. In the examples, all temperatures are in degrees Celsius (unless otherwise indicated). The compounds that have been prepared in accordance with the invention along with their biological activity data are presented in following Table. The syntheses of these representative compounds are carried out in accordance with the methods set forth above.

Exemplary Compounds of the Invention

The following compounds have been or can be prepared according to the synthetic methods described herein for example, method A-K. For the purpose of Table 1 below, activity of each compound, which can be determined using the IL-1β assay method described in Example 9, is expressed as follows:

-   “+” compound exhibited 0-25% inhibition at 0.3 μM concentration -   “++” compound exhibited 26-50% inhibition at 0.3 μM concentration -   “+++” compound exhibited 51-75% inhibition at 0.3 μM concentration -   “++++” compound exhibited 76% or greater inhibition at 0.3 μM     concentration -   “*” compound exhibited 0-25% inhibition at 0.1 μM concentration -   “**” compound exhibited 26-50% inhibition at 0.1 μM concentration -   “***” compound exhibited 51-75% inhibition at 0.1 μM concentration -   “****” compound exhibited 76% or greater inhibition at 0.1 μM     concentration

Compounds with a percent inhibition represented by “++++” or “****” are of particular interest.

TABLE 1 IL-1β % Inhibition of Exemplary Compounds IL-1β % Inhib. ID Structure MW MS (obs) @ 0.3 μM 1001

379.46 380.00 +++ 1002

377.49 378.20 ++++ 1003

363.46 364.20 + 1004

383.88 384.10 ++++ 1005

363.46 364.40 ++++ 1006

335.40 336.40 + 1007

349.43 350.90 + 1008

413.50 414.20 1009

441.55 442.20 + 1010

456.58 457.80 + 1011

471.55 472.20 + 1012

457.52 457.70 ++ 1013

446.54 447.50 ++++ 1014

486.37 487.00 ++ 1015

400.47 401.00 ++++ 1016

432.40 433.10 ++++ 1017

383.88 384.00 ++ 1018

367.42 367.60 + 1019

349.43 350.20 + 1020

377.49 377.80 + 1021

379.46 380.56 ++++ 1022

409.48 410.20 + 1023

433.29 434.50 ++++ 1024

312.41 313.20 ++++ 1025

422.48 423.31 + 1026

428.49 429.32 ** 1027

420.51 421.18 + 1028

404.51 405.50 + 1029

426.90 427.03 + 1030

406.48 407.40 + 1031

424.93 425.11 ++ 1032

434.49 435.28 + 1033

410.90 411.09 + 1034

355.48 356.55 ** 1035

401.46 402.30 * 1036

391.51 392.40 + 1037

397.90 398.24 + 1038

407.47 408.32 + 1039

421.49 422.30 * 1040

443.50 444.45 + 1041

435.52 436.53 * 1042

419.52 420.24 + 1043

441.91 442.20 + 1044

421.49 422.25 + 1045

439.94 440.40 + 1046

449.50 450.40 + 1047

354.49 355.57 * 1048

376.50 377.44 * 1049

392.50 393.35 + 1050

390.52 391.40 + 1051

376.50 377.47 + 1052

398.89 399.14 + 1053

378.47 379.45 + 1054

396.92 397.27 + 1055

406.48 407.58 + 1056

382.89 383.41 + 1057

320.39 321.25 * 1058

336.39 337.37 + 1059

382.41 383.39 * 1060

366.41 367.34 + 1061

342.44 343.34 + 1062

364.44 365.38 ** 1063

388.42 389.28 * 1064

380.44 381.46 * 1065

378.47 379.44 + 1066

364.44 365.36 + 1067

386.83 387.19 ++ 1068

366.41 367.34 + 1069

384.86 385.44 ++++ 1070

394.42 395.27 + 1071

370.83 371.08 + 1072

415.45 416.31 + 1073

399.45 400.39 + 1074

421.45 422.15 + 1075

413.47 414.30 + 1076

411.50 412.54 + 1077

397.48 398.16 + 1078

419.87 420.17 + 1079

417.89 418.40 + 1080

427.46 428.15 + 1081

403.87 404.34 + 1082

396.87 397.20 ++ 1083

431.32 431.10 + 1084

431.32 431.10 + 1085

376.45 377.33 + 1086

390.48 391.50 + 1087

390.48 391.50 + 1088

390.48 391.50 + 1089

422.48 423.20 + 1090

376.45 377.33 + 1091

406.48 407.40 + 1092

418.53 419.38 + 1093

390.48 391.50 + 1094

420.51 421.17 + 1095

420.51 421.39 + 1096

412.49 413.40 + 1097

426.51 427.44 + 1098

412.49 413.40 + 1099

406.48 407.60 + 1100

436.51 437.58 + 1101

390.48 391.39 + 1102

406.48 407.61 + 1103

436.51 437.56 + 1104

390.48 391.38 + 1105

406.48 407.58 + 1106

420.51 421.39 + 1107

390.48 391.39 + 1108

404.51 405.53 + 1109

402.45 403.30 + 1110

420.46 421.37 + 1111

436.51 437.58 + 1112

420.51 421.38 + 1113

410.90 411.52 + 1114

410.90 411.49 + 1115

394.51 395.33 ++ 1116

406.52 407.60 + 1117

420.46 421.38 + 1118

434.49 435.55 + 1119

432.54 433.44 + 1120

410.90 411.52 + 1121

404.51 405.52 + 1122

380.49 381.48 + 1123

436.51 437.57 + 1124

394.44 395.28 + 1125

424.93 425.10 + 1126

420.51 421.39 + 1127

420.51 421.39 + 1128

410.90 411.51 + 1129

410.90 411.50 + 1130

404.51 405.51 + 1131

436.89 437.41 + 1132

410.90 411.50 + 1133

406.48 407.59 + 1134

418.53 419.49 + 1135

424.93 425.11 + 1136

418.53 419.40 + 1137

369.85 370.14 + 1138

404.30 404.37 + 1139

404.30 404.38 + 1140

363.46 364.41 + 1141

363.46 364.40 + 1142

363.46 364.40 + 1143

404.30 404.37 + 1144

395.46 396.18 + 1145

349.43 350.32 + 1146

379.46 380.56 * 1147

391.51 392.43 + 1148

363.46 364.40 + 1149

393.48 394.35 * 1150

393.48 394.37 + 1151

385.46 386.35 + 1152

399.49 400.42 + 1153

385.46 386.35 + 1154

367.42 368.27 + 1155

383.88 384.50 + 1156

409.48 410.56 + 1157

363.46 364.40 + 1158

409.48 410.49 + 1159

363.46 364.41 + 1160

393.48 394.36 + 1161

377.49 378.50 + 1162

375.43 376.29 + 1163

393.44 394.34 + 1164

409.48 410.50 + 1165

393.48 394.36 + 1166

383.88 384.50 + 1167

367.49 368.31 ++ 1168

379.50 380.57 + 1169

393.44 394.35 + 1170

407.47 408.50 + 1171

405.52 406.56 + 1172

383.88 384.50 + 1173

377.49 378.49 + 1174

353.46 354.52 + 1175

367.42 368.26 + 1176

397.90 398.10 + 1177

393.48 394.37 + 1178

393.48 394.36 + 1179

383.88 384.51 + 1180

383.88 384.49 + 1181

377.49 378.48 + 1182

409.87 410.41 + 1183

383.88 384.49 + 1184

379.46 380.56 + 1185

391.51 392.41 + 1186

397.90 398.24 +++ 1187

391.51 392.40 + 1188

411.89 412.20 + 1189

446.33 446.16 + 1190

446.33 446.16 + 1191

391.47 392.40 + 1192

405.50 406.47 ++ 1193

405.50 406.48 + 1194

405.50 406.48 + 1195

446.33 446.38 * 1196

437.49 438.60 * 1197

391.47 392.38 * 1198

421.49 422.34 * 1199

433.55 434.63 * 1200

405.50 406.64 + 1201

435.52 436.50 * 1202

435.52 436.54 + 1203

441.53 442.31 + 1204

409.46 410.51 + 1205

425.91 426.22 + 1206

421.49 422.35 + 1207

451.52 452.22 + 1208

405.50 406.61 + 1209

421.49 422.36 + 1210

451.52 452.20 + 1211

405.50 406.62 + 1212

421.49 422.38 + 1213

435.52 436.55 + 1214

405.50 406.63 + 1215

419.52 420.47 + 1216

417.46 418.42 + 1217

435.48 436.49 + 1218

451.52 452.22 ++ 1219

435.52 436.54 ++ 1220

425.91 426.26 + 1221

425.91 426.23 + 1222

409.53 410.57 + 1223

421.54 422.41 + 1224

435.48 436.48 + 1225

449.50 450.41 + 1226

447.56 448.38 + 1227

425.91 426.24 + 1228

419.52 420.46 + 1229

395.50 396.32 + 1230

451.52 452.23 + 1231

409.46 410.51 + 1232

439.94 440.40 + 1233

435.52 436.52 + 1234

435.52 436.53 + 1235

425.91 426.22 + 1236

425.91 426.21 + 1237

419.52 420.46 ++ 1238

451.91 452.15 ++ 1239

425.91 426.23 + 1240

421.49 422.34 ++ 1241

433.55 434.62 + 1242

439.94 440.40 ++ 1243

433.55 434.67 + 1244

368.86 368.99 + 1245

394.47 395.29 * 1246

348.44 349.37 * 1247

362.47 363.43 * 1248

392.50 393.35 + 1249

384.48 385.48 + 1250

398.50 399.26 + 1251

384.48 385.48 + 1252

366.43 367.34 + 1253

382.89 383.38 + 1254

378.47 379.44 + 1255

408.50 409.53 + 1256

362.47 363.40 + 1257

378.47 379.44 + 1258

408.50 409.55 + 1259

362.47 363.41 + 1260

378.47 379.45 + 1261

392.50 393.37 + 1262

362.47 363.40 + 1263

376.50 377.45 + 1264

374.44 375.20 + 1265

392.45 393.31 ++ 1266

408.50 409.54 + 1267

392.50 393.36 + 1268

382.89 383.38 + 1269

382.89 383.40 + 1270

366.50 367.36 + 1271

378.51 379.48 + 1272

392.45 393.32 + 1273

406.48 407.59 + 1274

404.53 405.45 + 1275

382.89 383.38 + 1276

376.50 377.45 + 1277

352.48 353.62 ++++ 1278

408.50 409.52 + 1279

366.43 367.35 + 1280

392.50 393.36 + 1281

392.50 393.37 ++ 1282

382.89 383.40 + 1283

382.89 383.23 ++ 1284

376.50 377.33 + 1285

408.88 409.24 + 1286

390.52 391.50 + 1287

396.92 397.26 + 1288

390.52 391.41 + 1289

306.36 307.20 + 1290

338.36 339.36 * 1291

322.36 323.47 + 1292

306.36 307.32 + 1293

336.39 337.43 + 1294

310.33 311.44 + 1295

322.36 323.54 + 1296

306.36 307.38 + 1297

322.36 323.55 ++ 1298

306.36 307.39 + 1299

322.36 323.55 + 1300

318.33 319.41 + 1301

336.35 337.42 + 1302

310.39 311.52 + 1303

322.41 323.56 + 1304

336.35 337.41 + 1305

350.37 351.47 + 1306

296.37 297.51 + 1307

336.39 337.36 + 1308

352.78 353.17 + 1309

340.81 341.31 ++++ 1310

336.39 337.36 + 1311

380.44 381.47 + 1312

372.42 373.32 + 1313

396.44 397.28 * 1314

396.44 397.27 + 1315

350.42 351.48 + 1316

366.41 367.34 + 1317

380.44 381.48 + 1318

350.42 351.48 + 1319

364.44 365.37 + 1320

362.38 363.27 + 1321

380.40 381.45 + 1322

396.44 397.27 + 1323

380.44 381.48 + 1324

370.83 371.09 ++ 1325

370.83 371.09 ++ 1326

354.45 355.53 ++++ 1327

366.46 367.36 + 1328

394.42 395.27 + 1329

392.48 393.25 + 1330

370.83 371.10 + 1331

364.44 365.37 + 1332

340.42 341.39 + 1333

396.44 397.20 + 1334

354.38 355.22 + 1335

384.86 385.13 + 1336

380.44 381.30 + 1337

380.44 381.30 + 1338

364.44 365.32 + 1339

370.83 371.10 + 1340

366.41 367.12 + 1341

378.47 379.37 + 1342

384.86 385.43 + 1343

378.47 379.45 + 1344

389.84 390.23 ++ 1345

383.45 384.53 + 1346

415.45 416.34 *** 1347

383.45 384.50 ** 1348

413.47 414.34 * 1349

413.47 414.33 * 1350

419.48 420.42 * 1351

399.45 400.40 + 1352

429.47 430.32 + 1353

399.45 400.41 + 1354

429.47 430.35 + 1355

399.45 400.40 + 1356

383.45 384.51 + 1357

397.48 398.13 + 1358

395.42 396.21 + 1359

413.43 414.29 ++ 1360

429.47 430.36 ++ 1361

413.47 414.31 + 1362

399.49 400.41 + 1363

413.43 414.31 + 1364

427.46 428.36 + 1365

429.47 430.36 + 1366

413.47 414.35 ++ 1367

413.47 414.33 + 1368

403.87 404.40 + 1369

397.48 398.12 + 1370

403.87 404.40 + 1371

399.45 400.37 + 1372

411.50 412.54 + 1373

396.53 397.10 ++++ 1374

514.42 515.20 ++++ 1375

384.47 385.10 ++++ 1376

514.42 515.00 + 1377

422.43 423.30 + 1378

500.39 501.30 +++ 1379

370.45 371.10 ++++ 1380

466.84 467.30 ++++ 1381

433.29 433.10 ++++ 1382

500.39 501.20 ++ 1383

456.52 457.00 + 1384

442.49 443.30 + 1385

451.87 452.00 ++++ 1386

418.32 417.90 +++ 1387

418.02 418.30 +++ 1388

385.50 385.60 + 1389

369.51 370.00 ++ 1390

427.59 428.20 ++++ 1391

397.90 398.20 ++++ 1392

405.28 405.00 +++ 1393

414.54 415.20 ++++ 1394

406.48 407.61 * 1395

382.50 383.44 * 1396

404.51 405.54 * 1397

395.46 396.31 * 1398

379.46 380.56 * 1399

377.49 378.51 * 1400

393.48 394.36 ** 1401

377.49 378.51 * 1402

399.88 400.35 * 1403

437.49 438.60 * 1404

419.52 420.46 * 1405

378.47 379.46 * 1406

397.48 399.33 * 1407

399.45 400.40 * 1408

438.52 439.57 * 1409

379.46 380.55 * 1410

427.50 428.27 * 1411

427.50 428.38 * 1412

403.31 403.26 * 1413

348.44 349.35 * 1414

362.47 363.38 * 1415

378.47 379.45 * 1416

390.52 391.42 * 1417

396.92 397.29 ** 1418

378.47 379.46 * 1419

292.34 293.28 * 1420

306.36 307.32 * 1421

354.41 355.41 1422

352.39 353.34 * 1423

306.36 307.32 * 1424

322.36 323.46 * 1425

334.42 335.49 * 1426

350.42 351.47 * 1427

350.42 351.47 ** 1428

336.39 337.39 * 1429

366.41 367.33 * 1430

378.47 379.45 * 1431

350.42 351.47 * 1432

380.44 381.46 * 1433

386.45 387.26 * 1434

372.42 373.29 * 1435

354.38 355.19 * 1436

370.83 371.12 * 1437

366.41 367.35 * 1438

350.42 352.38 ** 1439

366.41 367.34 * 1440

370.83 371.10 * 1441

370.83 371.06 * 1442

424.29 424.22 * 1443

424.29 424.20 * 1444

399.45 399.33 * 1445

431.49 432.50 * 1446

411.50 412.56 * 1447

405.46 406.59 * 1448

405.46 406.42 * 1449

387.41 388.25 ** 1450

413.47 414.34 * 1451

403.87 404.35 * 1452

403.87 404.23 * 1453

425.51 426.18 * 1454

387.41 388.28 * 1455

417.89 418.39 * 1456

419.52 420.47 * 1457

417.55 418.50 * 1458

441.53 442.37 * 1459

433.55 434.43 ** 1460

444.36 444.35 * 1461

403.52 404.49 * 1462

403.52 404.38 * 1463

403.52 404.50 * 1464

435.52 436.58 * 1465

389.50 390.43 * 1466

403.52 404.37 * 1467

433.55 434.42 * 1468

433.55 434.65 * 1469

425.53 426.26 * 1470

439.56 440.43 * 1471

425.53 426.25 * 1472

449.55 450.43 * 1473

449.55 450.43 * 1474

419.52 420.46 * 1475

417.55 418.54 * 1476

415.49 416.40 * 1477

449.55 450.43 * 1478

423.94 424.14 * 1479

407.55 408.46 * 1480

447.53 448.37 * 1481

423.94 424.14 * 1482

417.55 418.51 ** 1483

393.53 394.37 ** 1484

449.55 450.42 * 1485

437.97 438.39 * 1486

423.94 424.15 * 1487

423.94 424.14 * 1488

417.55 418.53 * 1489

423.94 424.33 * 1490

419.52 420.47 * 1491

431.58 432.39 * 1492

437.97 438.60 * 1493

433.51 434.39 * 1494

409.53 410.57 * 1495

431.53 432.36 * 1496

455.51 456.17 * 1497

447.53 448.36 ** 1498

445.56 446.54 * 1499

431.53 432.59 * 1500

453.92 454.31 * 1501

451.95 452.17 * 1502

461.52 462.54 * 1503

437.92 438.55 * 1504

423.90 424.31 *** 1505

458.34 458.34 ** 1506

458.34 458.34 ** 1507

403.48 404.46 * 1508

417.51 418.44 * 1509

417.51 418.46 * 1510

417.51 418.43 * 1511

458.34 458.10 * 1512

449.50 450.27 * 1513

403.48 404.35 * 1514

433.51 434.39 * 1515

465.55 466.29 * 1516

445.56 446.48 * 1517

417.51 418.49 * 1518

447.53 448.37 * 1519

437.92 438.57 * 1520

463.53 464.55 * 1521

417.51 418.45 * 1522

433.51 434.61 * 1523

447.53 448.40 * 1524

417.51 418.47 * 1525

431.53 432.57 * 1526

429.47 430.35 * 1527

447.49 448.38 * 1528

463.53 464.55 * 1529

447.53 448.40 * 1530

437.92 438.54 ** 1531

453.92 454.22 ** 1532

433.55 434.63 * 1533

447.49 448.37 ** 1534

437.92 438.53 *** 1535

463.53 464.57 * 1536

421.47 422.32 * 1537

451.95 452.20 ** 1538

447.53 448.41 ** 1539

447.53 448.41 * 1540

437.92 438.57 * 1541

437.92 438.60 * 1542

431.53 432.59 * 1543

463.92 464.48 * 1544

437.92 438.58 * 1545

433.51 434.60 * 1546

445.56 446.56 * 1547

451.95 452.21 * 1548

482.46 483.35 * 1549

458.48 459.50 * 1550

480.48 481.40 * 1551

504.46 505.31 * 1552

496.48 497.40 * 1553

494.51 495.38 * 1554

480.48 481.38 * 1555

502.87 503.28 * 1556

482.46 483.35 * 1557

500.90 501.42 * 1558

510.47 511.35 * 1559

486.88 487.46 * 1560

472.85 473.40 * 1561

507.29 507.40 * 1562

452.43 453.24 * 1563

466.46 467.40 * 1564

466.46 467.40 * 1565

466.46 467.40 * 1566

498.45 499.37 ** 1567

452.43 453.17 * 1568

482.46 483.35 * 1569

514.50 515.61 * 1570

466.46 467.40 * 1571

496.48 497.34 * 1572

496.48 497.34 * 1573

502.49 503.33 * 1574

488.46 489.52 * 1575

470.42 471.38 * 1576

486.88 487.47 * 1577

482.46 483.36 * 1578

512.48 513.49 * 1579

466.46 467.40 * 1580

482.46 483.34 * 1581

512.48 513.49 * 1582

466.46 467.40 * 1583

482.46 483.35 ** 1584

496.48 497.35 * 1585

466.46 467.40 * 1586

480.48 481.39 * 1587

478.42 479.10 * 1588

496.44 497.32 * 1589

512.48 513.50 * 1590

496.48 497.21 ** 1591

486.88 487.47 * 1592

486.88 487.43 * 1593

470.49 471.45 * 1594

482.50 483.38 * 1595

496.44 497.34 * 1596

510.47 511.35 * 1597

508.52 509.36 * 1598

486.88 487.40 ** 1599

480.48 481.38 * 1600

456.46 457.36 * 1601

512.48 513.53 * 1602

470.42 471.40 * 1603

500.90 501.42 * 1604

496.48 497.34 * 1605

496.48 497.35 * 1606

480.48 481.39 * 1607

486.88 487.48 * 1608

482.46 483.34 * 1609

494.51 495.41 * 1610

500.90 501.39 * 1611

451.87 452.30 + 1612

425.96 426.20 + 1613

428.33 427.70 + 1614

437.97 438.10 + 1615

447.45 447.70 + 1616

447.45 447.40 + 1617

500.39 501.50 ++ 1618

485.43 485.60 + 1619

481.63 482.20 ++++ 1620

564.00 564.00 ++++ 1621

564.00 564.00 ++++ 1622

449.50 450.10 + 1623

438.83 439.20 ++++ 1624

539.86 540.10 ++ 1625

420.53 421.20 + 1626

523.41 524.30 + 1627

455.41 455.90 ++ 1628

471.86 472.30 ++++ 1629

434.55 435.20 ++ 1630

486.90 487.00 ++++ 1631

432.93 433.10 + 1632

453.34 453.10 ++ 1633

469.44 468.30 ++++ 1634

451.45 451.80 +++ 1635

469.44 470.20 ++++ 1636

466.37 466.10 ** 1637

435.88 437.30 ** IC₅₀ Determinations

The compounds set forth in Table 1 were tested for activity in a cellular model as described herein. Specifically, cells were pretreated with differing amounts of the compound under test and released IL-1β determined as in Example 9, above. Measurements were made and IC₅₀ values, presented in Table 2, below, were determined by fitting the data to a four parameter logistic equation using GraphPad Prism software (GraphPad Software, Inc). The equation may be expressed by the following formula: Y=Bottom+(Top−Bottom)/(1+10^((Log EC50−X)*HillSlope)) Where X is the logarithm of concentration, Y is the response and Y starts at Bottom and goes to Top with a sigmoid shape.

TABLE 2 IL-1β IC₅₀ for Exemplary Compounds IL-1β IC₅₀ ID (nM) 1001 240 1002 72.33 1003 >1000 1004 108.4 1005 39.59 1006 99.22 1007 >1000 1008 >1000 1009 >1000 1010 >1000 1011 >1000 1012 421.5 1013 0.355 1014 326.2 1015 171.1 1016 338.5 1017 367.5 1018 >1000 1019 >1000 1020 >1000 1021 >1000 1022 >1000 1023 53.45 1024 31.5 1366 409.6 1373 72.12 1374 40.57 1375 86.66 1376 731.3 1377 >1000 1378 120.8 1379 41.55 1380 5.332 1381 34.14 1382 602.3 1383 >1000 1384 >1000 1385 151.6 1386 237.9 1387 146.4 1388 >1000 1389 310.5 1390 79.25 1391 45.68 1392 123.1 1393 77.81 1611 929.7 1612 >1000 1613 >1000 1614 >1000 1615 >1000 1616 >1000 1617 417.5 1618 >1000 1619 67.18 1620 41.08 1621 6.864 1622 >1000 1623 9.24 1624 365 1625 >1000 1626 >1000 1627 416.1 1628 55.87 1629 456.6 1630 108.5 1631 >1000 1632 314.5 1633 25.54 1634 261.9 1635 111.7 Half-Life in Human Liver Microsomes (HLM)

Test compounds (1 μM) are incubated with 3.3 mM MgCl₂ and 0.78 mg/mL HLM (HL101) in 100 mM potassium phosphate buffer (pH 7.4) at 37° C. on the 96-deep well plate. The reaction mixture is split into two groups, a non-P450 and a P450 group. NADPH is only added to the reaction mixture of the P450 group. An aliquot of samples of P450 group is collected at 0, 10, 30, and 60 min time point, where 0 min time point indicated the time when NADPH is added into the reaction mixture of P450 group. An aliquot of samples of non-P450 group is collected at −10 and 65 min time point. Collected aliquots are extracted with acetonitrile solution containing an internal standard. The precipitated protein is spun down in centrifuge (2000 rpm, 15 min). The compound concentration in supernatant is measured by LC/MS/MS system.

The half-life value is obtained by plotting the natural logarithm of the peak area ratio of compounds/internal standard versus time. The slope of the line of best fit through the points yields the rate of metabolism (k). This is converted to a half-life value using following equations: Half-life=1n2/k Pharmacokinetic Evaluation of Compounds Following Intravenous and Oral Administration in Rats.

Male Sprague-Dawley rats are acclimatized for at least 24 hours prior to experiment initiation. During the acclimation period, all animals receive food and water ad libitum. However, food but not water is removed from the animals' cages at least 12 hours before initiation of the experiment. During the first 3 hours of experimentation, the animals receive only water ad libitum. At least three animals each are tested for intravenous and oral dosage. For intravenous formulation, compounds are dissolved (0.25 to 1 mg/mL) in a mixture of 3% dimethyl sulfoxide, 40% PEG 400 and the rest percentage of 40% Captisol in water (w/v). The animals are weighed before dosing. The determined body weight is used to calculate the dose volume for each animal. Dose volume (mL/kg)=1 mg/kg/formulation concentration (mg/mL) In instances where the formulation concentrations are less than 0.5 mg/mL, the dosing volume is about 2 mL/kg.

For oral formulation, compounds of this invention are suspended (0.5 to 0.75 mg/mL) in a mixture of 5% of 10% Tween 80 in water (v/v) and 95% of 0.5% methyl cellulose in water (w/v). PO rats are typically dosed through oral gavage following the same dose volume formula as IV to achieve a dose level of 1 to 5 mg/kg. For IV dosing, blood samples are collected (using a pre-heparinized syringe) via the jugular vein catheter at 2, 5, 15, 30, 60, 120, 180, 300, 480, and 1440 minutes post dosing. For PO dosing, blood samples are collected (using a pre-heparinized syringe) via the jugular vein catheter before dosing and at 5, 15, 30, 60, 120, 180, 300, 480, and 1440 minutes post dosing. About 250 uL of blood is obtained at each time point from the animal. Equal volumes of 0.9% normal saline are replaced to prevent dehydration. The whole blood samples are maintained on ice until centrifugation. Blood samples are then centrifuged at 14,000 rpm for 10 minutes at 4° C. and the upper plasma layer transferred into a clean vial and stored at −80° C. The resulting plasma samples are then analyzed by liquid chromatography-tandem mass spectrometry. Following the measurement of plasma samples and dosing solutions, plasma concentration-time curve is plotted. Plasma exposure is calculated as the area under the concentration-time curve extrapolated to time infinite (AUC_(inf)). The AUC_(inf) is averaged and the oral bioavailability (% F) for individual animal is calculated as: AUC_(inf)(PO)/AUC_(inf)(IV), normalized to their respective dose levels. The % F can be reported as the mean % F of all animals dosed orally with the compound of the invention at the specified level.

From the foregoing description, various modifications and changes in the compositions and methods of this invention will occur to those skilled in the art. All such modifications coming within the scope of the appended claims are intended to be included therein.

All publications, including but not limited to patents and patent applications, cited' in this specification are herein incorporated by reference as if each individual publication were specifically and individually indicated to be incorporated by reference herein as though fully set forth.

The chemical names of compounds of the invention given in this application are generated using Open Eye Software's Lexichem naming tool, Symyx Renaissance Software's Reaction Planner or MDL's ISIS Draw Autonom Software tool and not verified. 

What is claimed is:
 1. A bicycloheteroaryl compound having a formula:

wherein B and Y are independently selected from CR^(2a); W, W′ and Z are each independently CR⁴; L¹ is substituted or unsubstituted C₁C₅ alkylene; n is 1, 2, 3 or 4; R¹ is selected from a substituted or unsubstituted heterocycloalkyl, aryl and heteroaryl ring; each of R^(2a), R^(2′) and R^(2″) is independently selected from hydrogen, halo, and substituted or unsubstituted C₁-C₆ alkyl; or any of R^(2′) and R^(2″) join together to form a cycloalkyl or cycloheteroalkyl ring of 3-7 atoms; R³ is hydrogen or a functional group selected from acyl, substituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted dialkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, aryl, substituted aryl, arylalkyl, substituted or unsubstituted sulfone, substituted or unsubstituted sulfanyl, substituted or unsubstituted aminosulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted carbamoyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, halo, heteroaryloxy, substituted or unsubstituted heteroaryl, substituted or unsubstituted heteroalkyl, nitro, and thio; provided that R³ is other than hydrogen bond donor group; R⁴ is independently selected from H, alkyl, substituted alkyl, acyl, substituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, aryl, substituted aryl, arylalkyl, substituted or unsubstituted sulfone, substituted or unsubstituted sulfanyl, substituted or unsubstituted aminosulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted dihydroxyphosphoryl, azido, carboxy, substituted or unsubstituted carbamoyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroaryl, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thio; and the dotted bond is a double bond; or a pharmaceutically acceptable salt thereof; and stereoisomers, isotopic variants and tautomers thereof.
 2. A compound according to claim 1 wherein each of B and Y is CH; and the dotted bond is a double bond.
 3. A compound according to claim 1 wherein each of R^(2′) and R^(2″) is H.
 4. A compound according to claim 1 wherein one of R^(2′) and R^(2″) is independently Me and the other is H.
 5. A compound according to claim 1 wherein R¹ is substituted or unsubstituted aryl or substituted or unsubstituted heteroaryl.
 6. A compound according to claim 1 wherein R¹ is substituted or unsubstituted phenyl, pyridyl, quinoline, or benzodioxole, benzodioxane, benzofuran, benzothiophene, and benzodioxepine.
 7. A compound according to claim 1 wherein the compound is according to formula III or IV:

wherein W is CR⁴; Z is CR⁴; L¹, R¹, R^(2′), R^(2″), R³ and R⁴ are as in claim 1; and R⁵ is selected from H, alkyl, substituted alkyl, acyl, substituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, arylalkyl, substituted or unsubstituted sulfone, substituted or unsubstituted sulfanyl, substituted or unsubstituted aminosulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted dihydroxyphosphoryl, azido, carboxy, substituted or unsubstituted carbamoyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thio; or a pharmaceutically acceptable salt thereof; and stereoisomers, isotopic variants and tautomers thereof.
 8. A compound according to claim 1 wherein the compound is according to formula IX or X:

wherein W is CR⁴; Z is CR⁴; L¹, R³ and R⁴ are as in claim 1; R⁵ is selected from H, alkyl, substituted alkyl, acyl, substituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, arylalkyl, substituted or unsubstituted sulfone, substituted or unsubstituted sulfanyl, substituted or unsubstituted aminosulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted dihydroxyphosphoryl, azido, carboxy, substituted or unsubstituted carbamoyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thio; R^(2′) is H or Me; each R^(4a) is selected from hydrogen, alkyl, substituted alkyl, acyl, substituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, aryloxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, aryl, substituted aryl, arylalkyl, substituted or unsubstituted sulfone, substituted or unsubstituted sulfanyl, substituted or unsubstituted aminosulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted dihydroxyphosphoryl, azido, carboxy, substituted or unsubstituted carbamoyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroaryl, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thio; and m is selected from 0-5; or a pharmaceutically acceptable salt thereof; and stereoisomers, isotopic variants and tautomers thereof.
 9. A compound according to any one of claims 1,7 and 8, wherein L¹ is a C₁-C₅ alkylene unsubstituted or substituted by one or more substituents independently selected from alkyl and oxo.
 10. A compound according to any one of claims 1, 7 and 8, wherein R³ is selected from alkyl, dialkylamino, acyloxy, alkoxy, and —SO₂-alkyl.
 11. A compound according to any one of claims 1, 7 and 8, wherein R³ is selected from t-Bu, NMe₂, SO₂Me, OMe, and OCOMe.
 12. A compound according to any one of claims 1, 7 and 8, wherein R³ is substituted or unsubstituted aryl, heteroaryl, cycloalkyl or cycloheteroalkyl.
 13. A compound according to any one of claims 1, 7 and 8, wherein R³ is substituted or unsubstituted phenyl, pyridyl, pyran, tetrahydropyran, piperidine, morpholine, pyrrolidine, pyrrolidinone and benzodioxane.
 14. A compound according to any one of claims 1, 7 and 8, wherein the group -L₁-R³ is selected from


15. A compound according to claim 1 wherein the compound is according to formula XIa, XIb, XIc, XId, XIe, XIf, XIg, XIh or XIj:

wherein each R^(4a) is selected from hydrogen, alkyl, substituted alkyl, acyl, substituted acyl, substituted or unsubstituted acylamino, substituted or unsubstituted alkylamino, substituted or unsubstituted alkythio, substituted or unsubstituted alkoxy, aryloxy, alkoxycarbonyl, substituted alkoxycarbonyl, substituted or unsubstituted alkylarylamino, arylalkyloxy, substituted arylalkyloxy, amino, aryl, substituted aryl, arylalkyl, substituted or unsubstituted sulfone, substituted or unsubstituted sulfanyl, substituted or unsubstituted aminosulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted dihydroxyphosphoryl, azido, carboxy, substituted or unsubstituted carbamoyl, cyano, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloheteroalkyl, substituted or unsubstituted dialkylamino, halo, heteroaryloxy, substituted or unsubstituted heteroaryl, substituted or unsubstituted heteroalkyl, hydroxy, nitro, and thio; m is selected from 0-5; and R⁵ is selected from H, alkyl, or halo.
 16. A compound according to any one of claims 8 and 15, wherein m is 1 or 2; and each R^(4a) is independently selected from Me, Et, Ph, Cl, F, Br, CN, OH, OMe, OEt, OPh, COPh, CF₃, CHF₂, OCF₃, i-Pr, i-Bu, t-Bu, SMe, CH═CH—CO₂H, SOMe, SO₂Me, SO₃H, SO₃Me, and pyridyl.
 17. A compound according to any one of claims 1, 7 and 8, wherein each of W and Z is independently CH.
 18. A compound according to any one of claims 7, 8 and 15, wherein R⁵ is H, Me, Cl, F, or CF₃.
 19. A compound according to claim 1 wherein the compound is selected from table below: ID Structure 1001

1002

1003

1004

1005

1009

1010

1011

1016

1017

1018

1019

1020

1021

1022

1023

1027

1028

1031

1032

1036

1037

1038

1041

1042

1045

1046

1048

1049

1050

1051

1054

1055

1057

1058

1062

1064

1065

1066

1069

1070

1075

1076

1077

1079

1080

1093

1094

1095

1097

1099

1100

1101

1102

1103

1104

1105

1106

1107

1108

1110

1111

1119

1121

1123

1125

1126

1127

1130

1134

1135

1148

1149

1150

1152

1154

1155

1156

1157

1158

1159

1160

1161

1163

1164

1171

1173

1176

1177

1178

1181

1185

1186

1200

1201

1202

1203

1204

1205

1206

1207

1208

1209

1210

1211

1212

1213

1214

1215

1217

1218

1226

1228

1230

1232

1233

1234

1237

1241

1242

1247

1248

1250

1252

1253

1254

1255

1256

1257

1258

1259

1260

1261

1262

1263

1265

1266

1274

1276

1278

1280

1281

1284

1286

1287

1292

1293

1294

1295

1296

1297

1298

1299

1301

1307

1309

1311

1313

1314

1315

1316

1317

1318

1319

1321

1322

1329

1331

1333

1335

1336

1337

1338

1341

1342

1347

1348

1349

1350

1351

1352

1353

1354

1355

1356

1357

1359

1360

1365

1366

1367

1369

1374

1376

1377

1378

1380

1381

1382

1383

1384

1385

1386

1387

1391

1392

1396

1399

1400

1401

1404

1406

1409

1417

1422

1423

1431

1432

1433

1435

1436

1437

1438

1439

1449

1450

1453

1455

1457

1459

1466

1467

1468

1470

1472

1473

1474

1475

1477

1482

1484

1485

1488

1491

1492

1495

1497

1498

1499

1501

1502

1517

1518

1519

1520

1521

1522

1523  

1524

1525

1527

1528

1531

1535

1537

1538

1539

1542

1546

1547

1550

1552

1553

1554

1557

1558

1570

1571

1572

1573

1575

1576

1577

1578

1579

1580

1581

1582

1583

1584

1585

1586

1588

1589

1597

1599

1601

1603

1604

1605

1606

1609

1610

1611

1612

1613

1614

1615

1616

1617

1618

1620

1621

1623

1624

1626

1627

1628

1630

1631

1632

1633

1634

1635

1636

1637


20. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of a compound of claim
 1. 21. The pharmaceutical composition of claim 20, wherein the carrier is a parenteral, oral or topical carrier. 